@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY> .
@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:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_head {
  this: np:hasAssertion dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_assertion;
    np:hasProvenance dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_provenance;
    np:hasPublicationInfo dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_assertion a np:Assertion .
  
  dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_provenance a np:Provenance .
  
  dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C3494506 a ncit:C7057 .
  
  dgn-gda:DGN347e1b9cbd12e6de464951c1e772adc8 sio:SIO_000628 miriam-gene:5741, lld:C3494506;
    a sio:SIO_001121 .
}

dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_provenance {
  dgn-np:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_assertion dcterms:description
      "[Pseudohypoparathyroidism type Ia (PHP-Ia) is a hereditary disorder characterized by resistance to multiple hormones that work via cAMP such as PTH and TSH, accompanied by typical skeletal features including short stature and brachydactyly, termed Albright hereditary osteodystrophy (AHO).]. 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:17803690;
    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:NP628567.RAQebB02_ZaCGKZlh2ATG4oTeCrob2DQyH3YsD3dRKfOY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:30+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" .
}