@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc> .
@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:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_head {
  this: np:hasAssertion dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_assertion;
    np:hasProvenance dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_provenance;
    np:hasPublicationInfo dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_assertion a np:Assertion .
  
  dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_provenance a np:Provenance .
  
  dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_assertion {
  miriam-gene:80347 a ncit:C16612 .
  
  lld:C2931404 a ncit:C7057 .
  
  dgn-gda:DGN9d33a3d73f04afca60524e5ee19ed284 sio:SIO_000628 miriam-gene:80347, lld:C2931404;
    a sio:SIO_001121 .
}

dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_provenance {
  dgn-np:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_assertion dcterms:description
      "[Most individuals with Albright's hereditary osteodystrophy (AHO) have deficient expression or function of G(s alpha), the alpha subunit of the guanine nucleotide binding protein that stimulates adenylyl cyclase, and are resistant to parathyroid hormone (PTH) and other hormones that act via stimulation of adenylyl cyclase.]. 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:9506735;
    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:NP664706.RAb7J5BZmSg9Qg4P-sUlwoHKXXLpwHGiDBZURmvEuuYyc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:41+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" .
}