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Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
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scientific article published on 01 February 1983
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rdf:type
Item
description
wetenschappelijk artikel
(nl)
наукова стаття, опублікована в лютому 1983
(uk)
im Februar 1983 veröffentlichter wissenschaftlicher Artikel
(de)
scientific article published on 01 February 1983
(en)
artículu científicu espublizáu en febreru de 1983
(ast)
publication date
wds:Q71654999-897D0410-CF3A-48D1-A419-FE34A1B7DFBF
publication date
1983-02-01 00:00:00Z
(
xsd:dateTime
)
language of work or name
wds:Q71654999-EE88FA13-FC7F-49DE-9118-F7CFFA622A89
language of work or name
English
cites work
wds:Q71654999-1FDDF82A-D238-46D3-BC64-F75256511A96
wds:Q71654999-243C4417-31C1-4A26-9084-B569B30CA781
wds:Q71654999-D02F7884-0141-405A-9805-E2DD0BAF13AD
wds:Q71654999-E9AF068C-373B-4078-A2C8-FF386ABF30EC
wds:Q71654999-FEC2CE39-D683-4769-99F8-7CB30FCD2D92
cites work
Hypertelorism With Turner Phenotype
Factor XIII.
The measurement of factor XI (Plasma thromboplastin antecedent). Diagnosis and therapy of the congenital deficiency state.
The Noonan syndrome: a family study.
Noonan syndrome in an adult family presenting with chronic lymphedema
author name string
wds:Q71654999-8BBF349E-AA52-45EE-AF9C-8B36367BD6CD
wds:Q71654999-BCF66096-F67A-4068-A908-62830FB4D503
author name string
J A Alexander
C S Kitchens
rdfs:label
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(en)
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(nl)
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(sq)
skos:prefLabel
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(en)
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(nl)
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(sq)
name
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(en)
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(nl)
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(sq)
title
wds:Q71654999-205BB7DF-6C9F-4721-9ADF-C5F805247F35
title
Partial deficiency of coagulation factor XI as a newly recognized feature of Noonan syndrome
(en)
page(s)
wds:Q71654999-BC501D45-8BB2-4B7D-ACE6-E5A8F7138B4E
page(s)
224-227
instance of
wds:Q71654999-64AC39CF-7616-4B27-BCB8-8F14C4A82D38
instance of
scholarly article
main subject
wds:Q71654999-FD07A6C7-5020-4430-A820-D61022BD0ED3
main subject
Noonan syndrome
PubMed ID
wds:Q71654999-99C7F272-EA29-4432-8EC6-F299862D5DC4
PubMed ID
http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6822926
PubMed ID
6822926
published in
wds:Q71654999-15339A7C-57AC-42DC-B1B9-53E5B39EDD1E
published in
The Journal of Pediatrics
issue
wds:Q71654999-8D1CB348-FEF8-406C-A107-D853BA80E6AD
volume
wds:Q71654999-FAA59668-C1A9-4B40-80ED-B3E265438A81
issue
2
volume
102
DOI
wds:Q71654999-561727C9-B987-4950-A46B-CD8CEAA2F662
DOI
http://dx.doi.org/10.1016/S0022-3476(83)80525-3
DOI
10.1016/S0022-3476(83)80525-3
is
about
of
https://www.wikidata.org/wiki/Special:EntityData/Q71654999
is
cites work
of
Noonan syndrome
Occurrence of myeloproliferative disorder in patients with Noonan syndrome
CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes
Noonan's and DiGeorge syndromes with monosomy 22q11.
Evaluation of bleeding disorders in patients with Noonan syndrome: a systematic review
is
cites work
of
wds:Q33499657-9F0A3B33-9F1E-4012-ACD4-105C9554C4C1
wds:Q30829917-FE28EE4B-E30D-465C-9117-6D359310DAA9
wds:Q68929823-722A8E21-684D-4F75-8C0B-B021D2883EDC
wds:Q41904758-6E5FAB6E-A68B-4373-B5A2-02065D2937D8
wds:Q59126209-625DA2DC-42D9-4DC4-AF46-141F366EBAEF
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