About: Ada Hamosh

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

Attributes	Values
rdf:type	Item
rdfs:label	Ada Hamosh (en) Ada Hamosh (cs) Ada Hamosh (de) Ada Hamosh (es) Ada Hamosh (fr) Ada Hamosh (it) Ada Hamosh (nl) Ada Hamosh (pt) Ada Hamosh (sl) Ada Hamosh (pt-br) Ada Hamosh (ast)
skos:prefLabel	Ada Hamosh (en) Ada Hamosh (cs) Ada Hamosh (de) Ada Hamosh (es) Ada Hamosh (fr) Ada Hamosh (it) Ada Hamosh (nl) Ada Hamosh (pt) Ada Hamosh (sl) Ada Hamosh (pt-br) Ada Hamosh (ast)
name	Ada Hamosh (en) Ada Hamosh (cs) Ada Hamosh (de) Ada Hamosh (es) Ada Hamosh (fr) Ada Hamosh (it) Ada Hamosh (nl) Ada Hamosh (pt) Ada Hamosh (sl) Ada Hamosh (pt-br) Ada Hamosh (ast)
given name	wds:Q61639214-71fea0eb-40d7-bc10-d4c5-d34b84298cda
given name	Ada
instance of	wds:Q61639214-F9255A30-669B-4FC7-A2AD-744B5C814501
NL CR AUT ID	wds:Q61639214-544F5DEF-E76D-4EC2-B27C-437A28C1DBFC
instance of	Homo sapiens
NL CR AUT ID	xx0090285
Nationale Thesaurus voor Auteursnamen ID	wds:q61639214-bc3ae2c5-4208-2b5e-f826-e6b930de9fe0
NORAF ID	wds:q61639214-be4a2a6b-4852-83d9-c4b5-8d85fc54a744
occupation	wds:q61639214-00e64f61-4b2b-a398-69c4-c20b24282821
University of Barcelona authority ID	wds:Q61639214-97A12B1E-0FCA-4466-A428-9642D7050D0C
NUKAT ID	wds:Q61639214-A403138C-28F7-428E-BD6F-F37429E5D358
CONOR.SI ID	wds:Q61639214-51AF241F-E17A-40F6-A8AD-2CFAE5B36904
languages spoken, written or signed	wds:Q61639214-021D79D2-4B83-42B0-9BCE-00E3142019DC
University of Barc...D (former scheme)	wds:Q61639214-A48CFE4C-D4B6-4C36-B2E7-E02B90DBA2DE
sex or gender	wds:Q61639214-E480953B-9AE0-4643-8285-9C1A17E1D8F8
ISNI	wds:q61639214-287d618d-4877-a45a-07ec-7fd6c97e8456
VIAF ID	wds:Q61639214-51d2098b-4e2e-84c2-3b3c-9888a4b4b4e9
Library of Congress authority ID	wds:q61639214-4c91c6a7-4500-7398-ed0c-aa8df305331f
IdRef ID	wds:q61639214-44a46976-409f-0f2d-7690-0e6dccb6440a
National Library of Brazil ID	wds:q61639214-1a007492-4df9-13d0-dcaf-627c32ec79b5
family name	wds:q61639214-0e19a28a-4730-33f3-cf3e-68c43b896f8f
WorldCat Identities ID (superseded)	wds:q61639214-e9b6f408-4837-1027-76fc-dfb80751afe4
Canadiana Name Authority ID	wds:q61639214-1c3759a4-4e5e-2014-e268-e71cf257e214
National Library of Israel J9U ID	wds:q61639214-1e6fddb6-49f6-8791-7b33-c194b1b1f9bf
CANTIC ID	wds:Q61639214-9A00D74A-2F06-435A-9B33-4806D6224FC6
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p30413189X
NORAF ID	https://livedata.bibsys.no/authority/15037185
VIAF ID	http://viaf.org/viaf/163294141
Library of Congress authority ID	http://id.loc.gov/authorities/names/no2008119165
IdRef ID	http://www.idref.fr/143150979/id
Nationale Thesaurus voor Auteursnamen ID	30413189X
NORAF ID	15037185
occupation	physician
University of Barcelona authority ID	981058526992806706
NUKAT ID	n2007010394
CONOR.SI ID	133243747
languages spoken, written or signed	English
University of Barc...D (former scheme)	a1379640
sex or gender	female organism
ISNI	0000000117131486
VIAF ID	163294141
Library of Congress authority ID	no2008119165
IdRef ID	143150979
National Library of Brazil ID	000442280
family name	Hamosh
WorldCat Identities ID (superseded)	lccn-no2008119165
Canadiana Name Authority ID	ncf10963373
National Library of Israel J9U ID	987007459912905171
CANTIC ID	981058526992806706
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61639214
is author of	OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders Walking the interactome for candidate prioritization in exome sequencing studies of Mendelian diseases The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions. Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. The Matchmaker Exchange: a platform for rare disease gene discovery PhenoDB: a new web-based tool for the collection, storage, and analysis of phenotypic features GeneMatcher: a matching tool for connecting investigators with an interest in the same gene Problematic variation in local institutional review of a multicenter genetic epidemiology study Development of human protein reference database as an initial platform for approaching systems biology in humans Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders The Human Phenotype Ontology in 2017 Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies Getting ready for the Human Phenome Project: the 2012 forum of the Human Variome Project Heritability of lung disease severity in cystic fibrosis

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