@prefix orcid: . @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:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_head { this: np:hasAssertion dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_assertion; np:hasProvenance dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_provenance; np:hasPublicationInfo dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_publicationInfo; a np:Nanopublication . dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_assertion a np:Assertion . dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_provenance a np:Provenance . dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_publicationInfo a np:PublicationInfo . } dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_assertion { miriam-gene:535 a ncit:C16612 . lld:C1956346 a ncit:C7057 . dgn-gda:DGN12cc550f63b4ef79c963f39fb84c98bd sio:SIO_000628 miriam-gene:535, lld:C1956346; a sio:SIO_001122 . } dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_provenance { dgn-np:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_assertion dcterms:description "[In order to assess such relationships we have examined allele frequencies of 8 different RFLPs within or adjacent to the apo A-I, C-III and A-IV gene complex on the long arm of chromosome 11 (MspI, 5' to the apo A-I gene; MspI, within the apo A-I gene; PstI, 3' to the apo A-I gene; SstI, 3' to the apo C-III gene; PvuII, within the apo C-III gene; PvuII, 5' to the apo C-III gene; XbaI, within the apo A-IV gene; and XbaI, 3' to the apo A-IV gene) in 202 patients with CAD (50% narrowing of one or more coronary arteries) prior to age 60 and 145 normal controls.]. 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:1678604; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP256956.RArSodN_HVaO7igoSoGEM49_kIHUDSQHBfAb5zwoyrj9g130_publicationInfo { this: dcterms:created "2015-08-25T14:40:06+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X, orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654; pav:createdBy orcid:0000-0003-0169-8159; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }