@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_head {
  this: np:hasAssertion dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_assertion ;
    np:hasProvenance dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_provenance ;
    np:hasPublicationInfo dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_assertion a np:Assertion .
  dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_provenance a np:Provenance .
  dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  lld:C0018802 a ncit:C7057 .
  dgn-gda:DGN480bdf7e9f7223aa09ea4410d0f81664 sio:SIO_000628 miriam-gene:4846 , lld:C0018802 ;
    a sio:SIO_001121 .
}
dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_provenance {
  dgn-np:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_assertion dcterms:description "[Our findings suggest the possible implication of NOS3 gene in the disease phenotype, wherein NOS3 may be synergistically functioning in DCM associated heart failure via the excessive production of NO in cardiomyocytes resulting in decreased myocardial contractility and systolic dysfunction, a common feature of DCM phenotype.]. 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:23923002 ;
    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:NP1100387.RAPZlTddGRw3RxY9_l8Z11DyRDDsVxgxMTqfV_ARnn4QM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:04+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetv3.0rdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}