@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw> .
@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:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_head {
  this: np:hasAssertion dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_assertion;
    np:hasProvenance dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_provenance;
    np:hasPublicationInfo dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_assertion a np:Assertion .
  
  dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_provenance a np:Provenance .
  
  dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_assertion {
  miriam-gene:857 a ncit:C16612 .
  
  lld:C2973725 a ncit:C7057 .
  
  dgn-gda:DGN4ac255b905f37aeead0fcb87dccee66f sio:SIO_000628 miriam-gene:857, lld:C2973725;
    a sio:SIO_001121 .
}

dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_provenance {
  dgn-np:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_assertion dcterms:description
      "[We studied a family in which multiple members had pulmonary arterial hypertension without identifiable mutations in any of the genes known to be associated with the disease, including BMPR2, ALK1, ENG, SMAD9, and CAV1.]. 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:23883380;
    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:NP733407.RAzaCur7hMRVzLipySFVZZCRq4zyuIMnHaVFNnrPQ2hlw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:25+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" .
}