@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_head { this: np:hasAssertion dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_assertion; np:hasProvenance dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_provenance; np:hasPublicationInfo dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_publicationInfo; a np:Nanopublication . dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_assertion a np:Assertion . dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_provenance a np:Provenance . dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_publicationInfo a np:PublicationInfo . } dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_assertion { miriam-gene:3757 a ncit:C16612 . lld:C0023976 a ncit:C7057 . dgn-gda:DGN13bf69c6233935735fea6ccd05cd530c sio:SIO_000628 miriam-gene:3757, lld:C0023976; a sio:SIO_001121 . } dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_provenance { dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_assertion dcterms:description "[Among the genotype positive patients (N = 272), 243 had single pathogenic mutations (LQT1: n = 120 patients; LQT2: n = 93; LQT3: n = 26; LQT5: n = 3; LQT6: n = 1), and 29 patients (10% of genotype-positive patients and 5% overall) had two LQTS-causing mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:15840476; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP490714.RAZC_XGA_6dmuX_ZjRsFoOKchRh6wgqp_7BbADC7iDPZE130_publicationInfo { this: dcterms:created "2016-05-13T12:45:27+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }