@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:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_head { this: np:hasAssertion dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_assertion; np:hasProvenance dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_provenance; np:hasPublicationInfo dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_publicationInfo; a np:Nanopublication . dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_assertion a np:Assertion . dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_provenance a np:Provenance . dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_publicationInfo a np:PublicationInfo . } dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_assertion { miriam-gene:2263 a ncit:C16612 . lld:C0006142 a ncit:C7057 . dgn-gda:DGN0ddf151a36041ec8243e226f464e09bc sio:SIO_000628 miriam-gene:2263, lld:C0006142; a sio:SIO_001122 . } dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_provenance { dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_assertion dcterms:description "[A variant mapping to 10q26.13, approximately 300 kb telomeric to the established risk locus within the second intron of FGFR2, was also associated with breast cancer risk, although not at genome-wide statistical significance (rs10510102: OR = 1.12, 95% CI = 1.07 to 1.17, P = 1.58 × 10(-6)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_curated; sio:SIO_000772 miriam-pubmed:21263130; prov:wasDerivedFrom dgn-void:gwascat-2016; prov:wasGeneratedBy eco:ECO_0000218 . dgn-void:gwascat-2016 pav:importedOn "2016-01-27"^^xsd:date . dgn-void:source_evidence_curated a eco:ECO_0000205; rdfs:comment "Gene-disease associations manually curated."@en; rdfs:label "DisGeNET evidence - CURATED"@en . } dgn-np:NP52640.RAj3LvF8ul0fl7H0bkf2d8xZ9UV26KHL_waB6fxRlYPWU130_publicationInfo { this: dcterms:created "2016-05-13T12:42:12+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" . }