@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg> .
@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:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_head {
  this: np:hasAssertion dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_assertion;
    np:hasProvenance dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_provenance;
    np:hasPublicationInfo dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_assertion a np:Assertion .
  
  dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_provenance a np:Provenance .
  
  dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_assertion {
  miriam-gene:64805 a ncit:C16612 .
  
  lld:C0271623 a ncit:C7057 .
  
  dgn-gda:DGN3fc9574dbb8d9ae4141b8c26ecc51793 sio:SIO_000628 miriam-gene:64805, lld:C0271623;
    a sio:SIO_001121 .
}

dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_provenance {
  dgn-np:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_assertion dcterms:description
      "[Examples of drugs developed as a result of targeting GPCRs mutated in disease include: calcimimetics and calcilytics, therapeutics targeting melanocortin receptors in obesity, interventions that alter GNRHR loss from the cell surface in idiopathic hypogonadotropic hypogonadism and novel drugs that might rescue the P2RY12 receptor congenital bleeding 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:25150870;
    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:NP1213131.RAtM5mtVPvG9dJ25bO7qFSZ8WllDVUYvXkd8JX44KgrZg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:55+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" .
}