@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE> .
@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:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_head {
  this: np:hasAssertion dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_assertion;
    np:hasProvenance dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_provenance;
    np:hasPublicationInfo dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_assertion a np:Assertion .
  
  dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_provenance a np:Provenance .
  
  dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_assertion {
  miriam-gene:5744 a ncit:C16612 .
  
  lld:C0149911 a ncit:C7057 .
  
  dgn-gda:DGN8cc7f7b4096fbeb4a31e9f43d68021ef sio:SIO_000628 miriam-gene:5744, lld:C0149911;
    a sio:SIO_001121 .
}

dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_provenance {
  dgn-np:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_assertion dcterms:description
      "[Parathyroid hormone-related protein (PTHrP) is the causative factor of the paraneoplastic syndrome humoral hypercalcemia of malignancy (HHM) and it also contributes to osteolytic metastases, both of which are common complications of squamous carcinomas of the lung.]. 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:19825997;
    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:NP157838.RAhIBNB6C0s3hIpJFNiv_UkwrBE_RcNStUbfAfaEFTNtE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:25+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" .
}