@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw> .
@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:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_head {
  this: np:hasAssertion dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_assertion;
    np:hasProvenance dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_provenance;
    np:hasPublicationInfo dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_assertion a np:Assertion .
  
  dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_provenance a np:Provenance .
  
  dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_assertion {
  miriam-gene:5447 a ncit:C16612 .
  
  lld:C0220724 a ncit:C7057 .
  
  dgn-gda:DGN904512f16bf46a334b48faedd3498bf1 sio:SIO_000628 miriam-gene:5447, lld:C0220724;
    a sio:SIO_001121 .
}

dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_provenance {
  dgn-np:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_assertion dcterms:description
      "[Although causal mutations in the FGFR2 gene have been found in some patients, mutations in the electron donor enzyme P450 oxidoreductase gene (POR) have recently been found to cause ABS in other patients.]. 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:18853185;
    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:NP197791.RAanjjwsRmSHiGxL4WHTtm7-Yw0ObCYIT9Duph7NSFCJw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}