@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs> .
@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:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_head {
  this: np:hasAssertion dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_assertion;
    np:hasProvenance dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_provenance;
    np:hasPublicationInfo dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_assertion a np:Assertion .
  
  dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_provenance a np:Provenance .
  
  dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_assertion {
  miriam-gene:847 a ncit:C16612 .
  
  lld:C0003076 a ncit:C7057 .
  
  dgn-gda:DGNc59b4443e98c51e94ddcbf0183ee5eed sio:SIO_000628 miriam-gene:847, lld:C0003076;
    a sio:SIO_001121 .
}

dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_provenance {
  dgn-np:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_assertion dcterms:description
      "[However linkage analysis using tightly linked chromosome 11p13 markers flanking the aniridia locus (catalase, D11S151, and D11S325) made it highly unlikely that this patient inherited the aniridia gene from his affected mother.]. 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:1815167;
    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:NP156907.RAS9H1GpOTGLrdXrvL9eUsEa5lhY3w6Q22avY9KS4QwFs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:24+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" .
}