@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:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_head { this: np:hasAssertion dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_assertion; np:hasProvenance dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_provenance; np:hasPublicationInfo dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_publicationInfo; a np:Nanopublication . dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_assertion a np:Assertion . dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_provenance a np:Provenance . dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_publicationInfo a np:PublicationInfo . } dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_assertion { miriam-gene:1191 a ncit:C16612 . lld:C0494463 a ncit:C7057 . dgn-gda:DGN485e79fb087a1b90952182f0f1121d66 sio:SIO_000628 miriam-gene:1191, lld:C0494463; a sio:SIO_001121 . } dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_provenance { dgn-np:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_assertion dcterms:description "[This method will enable researchers to carry out genetic polymorphism studies for genetic risk factors associated with late-onset Alzheimer's disease (BIN1, CLU, ABCA7, CR1 and PICALM) without the use of expensive instrumentation and reagents.]. 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:23419238; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP275966.RAV2heEtVobISpX1Voe1gRZjPO4A2dp-pLbpcxNfX7gyg130_publicationInfo { this: dcterms:created "2014-10-02T12:34:35+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }