@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A> .
@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:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_head {
  this: np:hasAssertion dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_assertion;
    np:hasProvenance dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_provenance;
    np:hasPublicationInfo dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_assertion a np:Assertion .
  
  dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_provenance a np:Provenance .
  
  dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_assertion {
  miriam-gene:5741 a ncit:C16612 .
  
  lld:C0221357 a ncit:C7057 .
  
  dgn-gda:DGN2e70af786079c41d5537e4b915bb1550 sio:SIO_000628 miriam-gene:5741, lld:C0221357;
    a sio:SIO_001121 .
}

dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_provenance {
  dgn-np:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_assertion dcterms:description
      "[While loss-of-function mutations in Gsalpha are invariably associated with the short stature and brachydactyly of Albright hereditary osteodystrophy (AHO), the association with hormone resistance (to parathyroid hormone and thyrotropin) typical of pseudohypoparathyroidism type Ia (PHP-Ia) is much more variable.]. 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:9600732;
    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:NP522331.RAGoyHyfTRepZ2vqst0aJHBBoC5aG84qAAloJWhIxLl2A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}