@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:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_head { this: np:hasAssertion dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_assertion; np:hasProvenance dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_provenance; np:hasPublicationInfo dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_publicationInfo; a np:Nanopublication . dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_assertion a np:Assertion . dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_provenance a np:Provenance . dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_publicationInfo a np:PublicationInfo . } dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_assertion { miriam-gene:185 a ncit:C16612 . lld:C0853879 a ncit:C7057 . dgn-gda:DGN04b8f829fcaff67e260e08f436473059 sio:SIO_000628 miriam-gene:185, lld:C0853879; a sio:SIO_001122 . } dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_provenance { dgn-np:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_assertion dcterms:description "[The I/D and A1166C polymorphisms were evaluated by using polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP), respectively in 70 breast cancer patients diagnosed with invasive breast cancer and 70 healthy women.]. 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:20945417; 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:NP845551.RAE0VZT_ycj2zS9beS-g1XPLuqLooPrtjPtb3uFo_sceo130_publicationInfo { this: dcterms:created "2016-05-13T12:48:08+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" . }