@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:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_head { this: np:hasAssertion dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_assertion; np:hasProvenance dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_provenance; np:hasPublicationInfo dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_publicationInfo; a np:Nanopublication . dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_assertion a np:Assertion . dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_provenance a np:Provenance . dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_assertion { miriam-gene:2160 a ncit:C16612 . lld:C0005779 a ncit:C7057 . dgn-gda:DGNc98785ccd62356e88b493bd79d5770ec sio:SIO_000628 miriam-gene:2160, lld:C0005779; a sio:SIO_001121 . } dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_provenance { dgn-np:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_assertion dcterms:description "[In the present study, the gene encoding FXI (F11) was analyzed by direct sequencing in 33 individuals belonging to 11 unrelated Turkish families, and the bleeding tendency was quantitatively assessed by means of a bleeding questionnaire in 27 individuals with low FXI clotting activity and/or mutated F11 gene.]. 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:25158988; 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:NP1214005.RAHqaTJvcOtHNyxwA4ld_rTNm4xE0UdnGveNaOsxAWQPw130_publicationInfo { this: dcterms:created "2016-05-13T12:50:56+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" . }