@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:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_head { this: np:hasAssertion dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_assertion; np:hasProvenance dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_provenance; np:hasPublicationInfo dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_publicationInfo; a np:Nanopublication . dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_assertion a np:Assertion . dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_provenance a np:Provenance . dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_publicationInfo a np:PublicationInfo . } dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_assertion { miriam-gene:1934 a ncit:C16612 . lld:C0162429 a ncit:C7057 . dgn-gda:DGN417ef732c08c9c367da05544e9f3370a sio:SIO_000628 miriam-gene:1934, lld:C0162429; a sio:SIO_001121 . } dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_provenance { dgn-np:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_assertion dcterms:description "[Over the past 20 years, patients have been reported with GPVI-related defects involving: (i) an acquired deficiency, resulting from (a) anti-GPVI autoantibodies or (b) other causes; or (ii) a congenital deficiency, where (c) GPVI is not expressed or (d) is expressed in a dysfunctional form with defective signalling to alpha(IIb)beta(3).]. 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:17910626; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP366579.RAn6ED-4ihUeNOf06W3E-HJXk303iGbqfCpvN2LkCRx9w130_publicationInfo { this: dcterms:created "2015-08-25T14:41:11+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }