@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw> .
@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:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_head {
  this: np:hasAssertion dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_assertion;
    np:hasProvenance dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_provenance;
    np:hasPublicationInfo dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_assertion a np:Assertion .
  
  dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_provenance a np:Provenance .
  
  dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_assertion {
  miriam-gene:138428 a ncit:C16612 .
  
  lld:C0221357 a ncit:C7057 .
  
  dgn-gda:DGNa2f2265f5affa5db0b86da8b8fb57a16 sio:SIO_000628 miriam-gene:138428, lld:C0221357;
    a sio:SIO_001121 .
}

dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_provenance {
  dgn-np:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_assertion dcterms:description
      "[Albright's hereditary osteodystrophy (AHO) is characterized by phenotypic signs that typically include brachydactyly and sc calcifications occurring with or without hormone resistance toward PTH or other hormones such as thyroid hormone or gonadotropins.]. 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:11600516;
    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:NP350527.RARxUDUPiLJUI4nKhMZlpK7NanH833_eqjyA4z_IthICw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:25+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" .
}