@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:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_head { this: np:hasAssertion dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_assertion; np:hasProvenance dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_provenance; np:hasPublicationInfo dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_publicationInfo; a np:Nanopublication . dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_assertion a np:Assertion . dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_provenance a np:Provenance . dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_publicationInfo a np:PublicationInfo . } dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_assertion { miriam-gene:3673 a ncit:C16612 . lld:C0027051 a ncit:C7057 . dgn-gda:DGN929ea8c0be1b0f5e8faf6602c455ea32 sio:SIO_000628 miriam-gene:3673, lld:C0027051; a sio:SIO_001122 . } dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_provenance { dgn-np:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_assertion dcterms:description "[To determine the frequency of C807T polymorphism of the GPIa gene in young survivors of myocardial infarction (MI) and 2. to evaluate the relationship between the intensity of CAD in the coronary angiography examination and the 807C/T genetic status of the patients.]. 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:16136407; 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:NP511652.RAfgfgXEssnGR6HBhUU9HpbmkrIvXOdXm4foZ59WsWDnM130_publicationInfo { this: dcterms:created "2016-05-13T12:45:36+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" . }