@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:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_head { this: np:hasAssertion dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_assertion; np:hasProvenance dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_provenance; np:hasPublicationInfo dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_publicationInfo; a np:Nanopublication . dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_assertion a np:Assertion . dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_provenance a np:Provenance . dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_publicationInfo a np:PublicationInfo . } dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_assertion { miriam-gene:348 a ncit:C16612 . lld:C0009460 a ncit:C7057 . dgn-gda:DGNc6d140b0a44f20929af699549f47577a sio:SIO_000628 miriam-gene:348, lld:C0009460; a sio:SIO_001121 . } dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_provenance { dgn-np:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_assertion dcterms:description "[We tested the hypothesis that the T-allelic variant of the CALHM1 rs2986017 polymorphism confers susceptibility to Alzheimer's disease in a Hungarian case-control sample that was also genotyped for apolipoprotein E. This study included 238 probable patients with Alzheimer's disease who met the diagnostic criteria for National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer's Disease and Related Disorders Association and 202 elderly healthy control participants.]. 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:21378601; 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:NP449591.RAVtBnnoBqkciGGkqZwXXsRHV1FuP_JlR27S9At4mj9C8130_publicationInfo { this: dcterms:created "2014-10-02T12:36:28+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" . }