@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:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_head { this: np:hasAssertion dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_assertion; np:hasProvenance dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_provenance; np:hasPublicationInfo dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_publicationInfo; a np:Nanopublication . dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_assertion a np:Assertion . dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_provenance a np:Provenance . dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_publicationInfo a np:PublicationInfo . } dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_assertion { miriam-gene:2317 a ncit:C16612 . lld:C1565489 a ncit:C7057 . dgn-gda:DGNff0ea712de0f01ee5ba4ea61a1dd1db6 sio:SIO_000628 miriam-gene:2317, lld:C1565489; a sio:SIO_001121 . } dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_provenance { dgn-np:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_assertion dcterms:description "[The study suggests that the possibility exists that some alleles, in the TAP genes, might confer susceptibility or protection in patients with ESRD which might prove to be helpful in identifying individuals at a higher risk for progressive renal insufficiency.]. 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:21440064; 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:NP882521.RAQesY66zvxh5Ul0Uyteb0Tho0ztEBObI-ExgM7R7Zo6k130_publicationInfo { this: dcterms:created "2016-05-13T12:48:24+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" . }