@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:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_head { this: np:hasAssertion dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion; np:hasProvenance dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_provenance; np:hasPublicationInfo dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_publicationInfo; a np:Nanopublication . dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion a np:Assertion . dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_provenance a np:Provenance . dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion { miriam-gene:6649 a ncit:C16612 . lld:C0151744 a ncit:C7057 . dgn-gda:DGN4c5d0077e2e449b108217264c4e20cb7 sio:SIO_000628 miriam-gene:6649, lld:C0151744; a sio:SIO_001122 . } dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_provenance { dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion dcterms:description "[Substitution of arginine by glycine at amino acid 213 (R213G) of its HBD was first identified in patients with heart failure, followed by many studies that focused on the role of this variant (SOD3(R213G)) in ischemic heart disease and cardiovascular disease.]. 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:25927599; 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:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_publicationInfo { this: dcterms:created "2016-05-13T12:51:27+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" . }