@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_head {
  this: np:hasAssertion dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion;
    np:hasProvenance dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_provenance;
    np:hasPublicationInfo dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion a np:Assertion .
  
  dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_provenance a np:Provenance .
  
  dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion {
  miriam-gene:5340 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
  dgn-gda:DGN795835d1bed915fde6f3e12a813a2454 sio:SIO_000628 miriam-gene:5340, lld:C0007222;
    a sio:SIO_001121 .
}

dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_provenance {
  dgn-np:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_assertion dcterms:description
      "[The less efficient proteolytic processing of the Pro370Leu protein by plasmin, coupled with the strong association of this variant with ethnicity, suggests that the Pro370Leu CHGA gene variant may contribute to the differential prevalence of cardiovascular disease across ethnic groups.]. 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:17991725;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP877058.RA7DZwN_rynjp_uSsnIRQQ3rmP6x17sJqN44DHYsY3c8A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}