This HTML5 document contains 67 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

PrefixIRI
wdthttp://www.wikidata.org/prop/direct/
wdtnhttp://www.wikidata.org/prop/direct-normalized/
schemahttp://schema.org/
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
wikibasehttp://wikiba.se/ontology#
phttp://www.wikidata.org/prop/
n12http://dx.doi.org/10.1253/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n4http://rdf.ncbi.nlm.nih.gov/pubchem/reference/
xsdhhttp://www.w3.org/2001/XMLSchema#
wdshttp://www.wikidata.org/entity/statement/
wdhttp://www.wikidata.org/entity/

Statements

Subject Item
wd:Q38032128
rdf:type
wikibase:Item
schema:description
2012 ആഗസ്റ്റ് 3 നു പ്രസിദ്ധീകരിച്ച ശാസ്ത്ര ലേഖനം artikull shkencor articol științific vitskapeleg artikkel مقالة علمية نشرت في 03 أغسطس 2012 scientific article published on 03 August 2012 vedecký článok article scientifique artículu científicu espublizáu en 2012 научная статья artigo científico wetenschappelijk artikel наукова стаття, опублікована в серпні 2012 article científic vetenskaplig artikel বৈজ্ঞানিক নিবন্ধ articolo scientifico научни чланак מאמר מדעי videnskabelig artikel vědecký článek scienca artikolo wissenschaftlicher Artikel artikel ilmiah vitenskapelig artikkel artigo científico artículo científico scientific article published on 03 August 2012 scientific article published on 03 August 2012 artigo científico bilimsel makale
p:P577
wds:Q38032128-4A9BCE39-EE9F-442C-A1FD-E5C0D54AA1FB
wdt:P577
2012-08-03T00:00:00Z
p:P2093
wds:Q38032128-58EC4AB2-3F64-486C-9A8F-BF2CA3232285 wds:Q38032128-BAC35D43-2FD3-4C6A-9F02-A68CEF04AD1A
wdt:P2093
Isao Shiraishi Hajime Ichikawa
rdfs:label
Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – . Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – . Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – .
skos:prefLabel
Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – . Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – . Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – .
schema:name
Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – . Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – . Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – .
p:P1476
wds:Q38032128-DF0DCBFA-F451-46F5-BF79-02E4A3ECD30E
wdt:P1476
Human heterotaxy syndrome – from molecular genetics to clinical features, management, and prognosis – .
p:P304
wds:Q38032128-3C4EA35F-0D95-4F22-A4A6-5900C3D42CD9
wdt:P304
2066-2075
p:P31
wds:Q38032128-E8501150-BAF9-495C-9C34-910119D1342B
wdt:P31
wd:Q13442814
p:P921
wds:Q38032128-DEC54ACB-0263-4005-BD07-11F10875E5C6
wdt:P921
wd:Q210506
p:P698
wds:Q38032128-EC0E3D72-C591-49B0-8B51-A7DBFEE993C9
wdtn:P698
n4:22864291
wdt:P698
22864291
p:P1433
wds:Q38032128-1122522B-5FDB-4A96-A00E-9F533DFB77B1
wdt:P1433
wd:Q1955928
p:P433
wds:Q38032128-03796072-8081-420B-B655-5F1C8EDEC435
p:P478
wds:Q38032128-1868A9A2-0FE0-4E98-A6F9-8366EDD6E4C7
wdt:P433
9
wdt:P478
76
p:P356
wds:Q38032128-49EB4E9A-2E78-402B-A031-860D8518717D
wdtn:P356
n12:CIRCJ.CJ-12-0957
wdt:P356
10.1253/CIRCJ.CJ-12-0957