@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA> .
@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:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_head {
  this: np:hasAssertion dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_assertion;
    np:hasProvenance dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_provenance;
    np:hasPublicationInfo dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_assertion a np:Assertion .
  
  dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_provenance a np:Provenance .
  
  dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_assertion {
  miriam-gene:3630 a ncit:C16612 .
  
  lld:C1839839 a ncit:C7057 .
  
  dgn-gda:DGNd2adc03c5a869d02732c4fb154dec4ea sio:SIO_000628 miriam-gene:3630, lld:C1839839;
    a sio:SIO_001121 .
}

dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_provenance {
  dgn-np:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_assertion dcterms:description
      "[Reanalysis of an Old Order Amish pedigree, to include several new individuals and two changes in clinical status, markedly reduces the probability of linkage between bipolar affective disorder and the Harvey-ras-1 oncogene and insulin loci on chromosome 11.]. 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:2682265;
    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:NP687809.RAIWzatirRlM66qYDXFPA8bcMMFkEmE09LCG9sNtse6DA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+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" .
}