About: Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 April 2002

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 2002 (uk) article scientifique publié en 2002 (fr) im April 2002 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 2002 (ast) scientific article published on 01 April 2002 (en)
publication date	wds:Q77880318-BA21AA42-092E-4B5D-9A43-DE5C96BCFFCB
publication date	2002-04-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q77880318-03528CD5-9E4C-4DCF-864F-85C6B4A8F3E0 wds:Q77880318-0A3C0111-C02D-4144-9E06-5B22C1DC4CF1 wds:Q77880318-1137F88C-1695-4880-83A6-490B05879E29 wds:Q77880318-1D9B21C9-C889-4054-97A6-B5230B994B05 wds:Q77880318-411EE434-3377-4151-8835-333530F56622 wds:Q77880318-58D5FFC3-CA5B-4BB2-9F3C-E9EFA26CF1E5 wds:Q77880318-85D59E52-CE4A-4180-9601-13E5B7D1EBE2 wds:Q77880318-9AAD0054-BCE4-47BA-9C7C-46492DFF0BBE wds:Q77880318-A12D2C6B-2860-47F7-B71B-3BF85C9C5DBF wds:Q77880318-B287B56C-F09C-4162-8DCF-7325B5D3CA3A wds:Q77880318-C2BA9E62-60B8-4F57-9E40-79664EE94871 wds:Q77880318-CF64FE05-C70E-44DA-897B-0A3203AD10D0 wds:Q77880318-D815C53F-4A8C-4AB8-89DC-617569F9B2CB
cites work	Large-scale genotyping of single nucleotide polymorphisms by Pyrosequencing? and validation against the 5?nuclease (Taqman�) assay Commercial molecular diagnostics in the U.S.: The Human Genome Project to the clinical laboratory Analysis of SNPs and other genomic variations using gel-based chips An update on conformation sensitive gel electrophoresis The load of genetic and partially genetic disorders in man. I. Congenital anomalies: estimates of detriment in terms of years of life lost and years of impaired life. DHPLC screening of cystic fibrosis gene mutations. SNP genotyping with fluorescence polarization detection New developments in high-throughput resequencing and variation detection using high density microarrays Making ends meet in genetic analysis using padlock probes Correlation of MFOLD-predicted DNA secondary structures with separation patterns obtained by capillary electrophoresis single-strand conformation polymorphism (CE-SSCP) analysis. A surface invasive cleavage assay for highly parallel SNP analysis Determining sequence length or content in zero, one, and two dimensions Mutation detection 2001: Sixth International Symposium on Mutations in the Human Genome, May 3-7, 2001, Bled, Slovenia.
rdfs:label	Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 (en) Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 (nl)
skos:prefLabel	Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 (en) Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 (nl)
name	Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 (en) Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 (nl)
title	wds:Q77880318-41729553-7270-4518-A10E-DC849F86ED58
title	Mutation detection 2001: Novel technologies, developments and applications for analysis of the human genome. Proceedings of the 6th International Symposium on Mutations in the Human Genome. Bled, Slovenia, 2001 (en)
page(s)	wds:Q77880318-DF1D39E7-8ABF-48E7-A10F-3D32868C4723
page(s)	313-463
instance of	wds:Q77880318-7F10FCFE-1B19-490E-9B6E-6433E6B66279
instance of	scholarly article
main subject	wds:Q77880318-0C3B78EA-9916-4DB8-9811-624600A378E7
main subject	Socialist Republic of Slovenia
PubMed ID	wds:Q77880318-ADA8E41A-6E01-4432-9ACB-34660F2EC470
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11933185
PubMed ID	11933185
published in	wds:Q77880318-A0464C69-FD45-4012-8F4B-B922D37C915D
published in	Human Mutation
issue	wds:Q77880318-0C1C76F2-F60B-4555-851B-AE924B06473E
volume	wds:Q77880318-189B5D6C-E531-4E91-8035-25352B21B3B6
issue	4
volume	19
DOI	wds:Q77880318-4C2F9C53-F9B0-46CD-8035-FF726B4E5FF5
DOI	http://dx.doi.org/10.1002/HUMU.10088
DOI	10.1002/HUMU.10088
Fatcat ID	wds:Q77880318-D5B350B0-65CE-4FCB-9CC6-00D84AD9B55B
Fatcat ID	release_fmlekbdvjbfy7oi2kes4jgdsk4
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q77880318
is cites work of	Significance of TP53 mutations in human cancer: a critical analysis of mutations at CpG dinucleotides The potential of electrophoretic mobility shift assays for clinical mutation detection Locus-specific mutation databases: pitfalls and good practice based on the p53 experience ThinPrep-processed fine-needle samples of breast are effective material for RNA- and DNA-based molecular diagnosis: application to p53 mutation analysis. Renewable Standard Reference Material for the Detection of TP53 Mutations Use of TP53 reference materials to validate mutations in clinical tissue specimens by single-strand conformational polymorphism analysis. Rapid denaturing high-performance liquid chromatography (DHPLC) for mutation scanning of the transforming growth factor beta3 gene using a novel proof-reading polymerase.
is cites work of	wds:Q54694528-8FAA6724-CB30-465E-8015-F68426A3750C wds:Q35078721-FA416AC0-AE67-4493-86D8-DCCA4A38BBDB wds:Q36619487-17BBFFB4-D11B-4F34-8BF0-8C60F292EED6 wds:Q40567737-73E3CA7F-74D8-46D9-9C38-4878B47E59F4 wds:Q59526197-9B742251-95E1-4F4A-A352-AE029A742ECF wds:Q40622803-1E002E7B-B084-4B98-802B-89D4A336DDD9 wds:Q44670956-8AEABD0A-0710-4CF3-8CBA-D037C778EDA8

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 180 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software