@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:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_head { this: np:hasAssertion dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion; np:hasProvenance dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_provenance; np:hasPublicationInfo dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_publicationInfo; a np:Nanopublication . dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion a np:Assertion . dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_provenance a np:Provenance . dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion { miriam-gene:348 a ncit:C16612 . lld:C0007222 a ncit:C7057 . dgn-gda:DGNc525c6970b6c9cb15be95433e11af137 sio:SIO_000628 miriam-gene:348, lld:C0007222; a sio:SIO_001121 . } dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_provenance { dgn-np:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_assertion dcterms:description "[The apoE polymorphism affects the serum lipoprotein levels, and the ESRD patients who are e4 and e2 allele carriers are more likely to present an atherogenic lipoprotein profile that may be a major factor associated with increased risk of CVD.]. 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:25155022; 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:NP1213632.RAcvZoWW5kAlyPnpkn-DCBztfzrKTT4SrcZmYXT9Z4TfY130_publicationInfo { this: dcterms:created "2016-05-13T12:50:56+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" . }