@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY> .
@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:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_head {
  this: np:hasAssertion dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_assertion;
    np:hasProvenance dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_provenance;
    np:hasPublicationInfo dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_assertion a np:Assertion .
  
  dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_provenance a np:Provenance .
  
  dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_assertion {
  miriam-gene:59 a ncit:C16612 .
  
  lld:C0042373 a ncit:C7057 .
  
  dgn-gda:DGNe4411c17c32732db2afc89bec5c8ee9c sio:SIO_000628 miriam-gene:59, lld:C0042373;
    a sio:SIO_001121 .
}

dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_provenance {
  dgn-np:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_assertion dcterms:description
      "[We also present the current evidence that both NF1 and ACTA2 mutations promote increased smooth muscle cell proliferation in vitro and in vivo, which leads us to propose that these diffuse and diverse vascular diseases are the outward signs of a more fundamental disease: a hyperplastic vasculomyopathy.]. 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:20130469;
    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:NP373750.RA16Jn_IFzw_lk0s1XPwh2PffhfkYvsvOUvgFpd6qpiRY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:39+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" .
}