http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#head http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#assertion http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#provenance http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#assertion http://rdf.disgenet.org/resource/gda/DGNfd8e8ce7af38a40984dd13d4551389d1 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/10804 http://rdf.disgenet.org/resource/gda/DGNfd8e8ce7af38a40984dd13d4551389d1 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C3665333 http://rdf.disgenet.org/resource/gda/DGNfd8e8ce7af38a40984dd13d4551389d1 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#provenance http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#assertion http://purl.org/dc/terms/description [Because in the human skin connexin 26 (Cx26) is co-expressed with other connexins, like Cx43 and Cx30, and as the KID syndrome is inherited as autosomal dominant condition, it is possible that KID mutations change the way Cx26 interacts with other co-expressed connexins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/25625422 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/dc/terms/created 2017-10-17T13:18:02+02:00 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1230333.RA4VQ2C6v9NoPoo-Bm3YYQ9u4LBZrfOhi2prCqYIap_LU http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0