This HTML5 document contains 118 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/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n10http://dx.doi.org/10.1038/
n11http://rdf.ncbi.nlm.nih.gov/pubchem/reference/
xsdhhttp://www.w3.org/2001/XMLSchema#
n13https://scigraph.springernature.com/pub.10.1038/
wdshttp://www.wikidata.org/entity/statement/
wdhttp://www.wikidata.org/entity/

Statements

Subject Item
wd:Q28118889
rdf:type
wikibase:Item
schema:description
vědecký článek publikovaný v roce 1998 научни чланак (објављен 1998/05/01) articolo scientifico наукова стаття, опублікована в травні 1998 1998 թուականի Մայիսին հրատարակուած գիտական յօդուած مقالة علمية (نشرت في مايو 1998) scientific journal article im Mai 1998 veröffentlichter wissenschaftlicher Artikel wetenschappelijk artikel (gepubliceerd op 1998/05/01) artículu científicu espublizáu en 1998 1998 թվականի մայիսին հրատարակված գիտական հոդված vedecký článok (publikovaný 1998/05/01)
p:P577
wds:Q28118889-EDD55841-2BFE-4A3E-96AC-3C81364EA440
wdt:P577
1998-05-01T00:00:00Z
p:P407
wds:Q28118889-A7130434-C61D-430F-BFE2-5449F0C243D5
wdt:P407
wd:Q1860
p:P2888
wds:Q28118889-D16093DB-7F90-4A83-9F9F-23CB2F1D738B
wdt:P2888
n13:ng0598-60
p:P2860
wds:Q28118889-4E067DB8-DE44-4C6F-981E-CCAFB0969742 wds:Q28118889-5339F92A-00C3-4886-9820-68E467AF9679 wds:Q28118889-57FDE22B-3A5E-4853-B833-6A261AF31ED5 wds:Q28118889-59412A90-9FB9-4859-8600-9637A30C692A wds:Q28118889-612F1A3C-86A9-47FC-BDAF-5E6A5FB2AF25 wds:Q28118889-642F7788-6679-4458-B5FD-1D2CFE47576A wds:Q28118889-07EA7935-B763-4368-B07F-9E809436DB15 wds:Q28118889-69FEEF86-9642-4D96-83AE-2B466A382EF5 wds:Q28118889-A7E3CC7A-E8A5-4267-AE72-F515846C490A wds:Q28118889-B3E1F2B1-D442-4DF9-A204-DF5AEBDAC27A wds:Q28118889-BAA6BCBC-B105-4806-BC4C-A84328CA48E2 wds:Q28118889-2ACF36AE-F8EA-4D77-B39D-780FD4ADFFC6 wds:Q28118889-2C9C93B0-B0A1-4120-ADD4-9F77EE9A7757 wds:Q28118889-3309F9C6-D68E-454C-8DAD-A10FE66A88F5
wdt:P2860
wd:Q34460479 wd:Q34385077 wd:Q24563196 wd:Q28299295 wd:Q29618515 wd:Q30829521 wd:Q29619441 wd:Q24314769 wd:Q48069330 wd:Q24563736 wd:Q37705478 wd:Q36221099 wd:Q28511714 wd:Q28300248
p:P2093
wds:Q28118889-D474B321-8198-4697-A457-573DBE133F25 wds:Q28118889-BAFF0A69-D6AD-4BEC-97E7-314D2850EFDA wds:Q28118889-F90BC110-B17F-471C-8368-969594F6A952 wds:Q28118889-FCC5ACA0-405C-4709-8344-1F5A8F90912E wds:Q28118889-F7DA2BB3-613B-45DA-A62C-727D665E224E wds:Q28118889-3C41CEE5-180D-49F6-B967-575D16B27AF2 wds:Q28118889-33AB6F17-36BB-4E08-8AC5-FF8CB066A699 wds:Q28118889-5F05ED10-6ADD-4C38-9AA1-0CC0592BDD01 wds:Q28118889-4FED3A9F-58F4-4CE0-8296-CEFBFA118F5A wds:Q28118889-87F7CA9B-9FE4-4423-80D1-9AA9FE8DE692 wds:Q28118889-7D5FC2D0-1C90-4D75-AF6E-4A68707560E5 wds:Q28118889-6E895ADC-6387-4109-845D-0F4C6C223267 wds:Q28118889-69AB5C90-7C7F-444B-901A-BC40B0332655 wds:Q28118889-B3B8261C-5CCC-4921-A792-D1DA07BE736A wds:Q28118889-A7556E81-BAB3-483A-86BE-D9C596E096CC wds:Q28118889-89BF2F5F-60A7-434D-9EA5-B48107DC81CE wds:Q28118889-2AC45EDB-28D7-439C-8706-8E5C7DC62750 wds:Q28118889-E41840BB-257D-4708-86CE-FDFB996EBAAC wds:Q28118889-DCFBD894-DC98-4AEE-A55F-A5F417E5E7D8 wds:Q28118889-DF487378-8FB8-4A66-B7D9-1768D07F61CB
wdt:P2093
F. Wachtler M. Verstreken P. K. Legan D. C. Hughes G. P. Richardson P. Coucke F. E. Offeciers R. J. Smith G. Van Camp T. Somers K. Verhoeven L. Van Laer P. Van Hauwe W. J. Kimberling P. J. Willems P. Van de Heyning P. J. Govaerts K. Kirschhofer I. Schatteman A. Chen
rdfs:label
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
skos:prefLabel
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
schema:name
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
p:P1476
wds:Q28118889-E97A0670-A129-4842-99CA-33872E9EC0AD
wdt:P1476
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment
p:P304
wds:Q28118889-4F4437E9-0BCB-469F-B354-6EBDB6E9EE0E
wdt:P304
60–62
p:P31
wds:Q28118889-7336D6C9-88CC-4639-A655-3411B9F40244
wdt:P31
wd:Q13442814
p:P921
wds:Q28118889-83065530-9EF1-46BD-956A-053F14CEA5B0
wdt:P921
wd:Q16035842
p:P698
wds:Q28118889-D6ADBBF3-F1C7-4CA3-8E3D-A07B440B09FB
wdtn:P698
n11:9590290
wdt:P698
9590290
p:P1433
wds:Q28118889-288E70E1-DBDC-4563-BF0E-5F695756613C
wdt:P1433
wd:Q976454
p:P433
wds:Q28118889-480EB572-66C2-434F-A49A-76801BD12176
p:P478
wds:Q28118889-AFF93BE5-A4D9-4A15-885F-9D5ABBCCC0CA
wdt:P433
1
wdt:P478
19
p:P356
wds:Q28118889-802D84B7-25FE-4129-B79C-D61EA93B9974
wdtn:P356
n10:NG0598-60
wdt:P356
10.1038/NG0598-60
p:P5875
wds:Q28118889-54DBFE5E-6619-4C83-8A80-9D5D99612D57
wdt:P5875
13694413