@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg> .
@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:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_head {
  this: np:hasAssertion dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_assertion;
    np:hasProvenance dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_provenance;
    np:hasPublicationInfo dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_assertion a np:Assertion .
  
  dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_provenance a np:Provenance .
  
  dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_assertion {
  miriam-gene:51684 a ncit:C16612 .
  
  lld:C0206656 a ncit:C7057 .
  
  dgn-gda:DGN9de98331c7f6981f997ce2af3ad9a429 sio:SIO_000628 miriam-gene:51684, lld:C0206656;
    a sio:SIO_001121 .
}

dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_provenance {
  dgn-np:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_assertion dcterms:description
      "[Four of nine informative fetal rhabdomyomas and embryonal rhabdomyosarcomas showed loss of heterozygosity (LOH) in the PTCH region with two of these (one fetal rhabdomyoma and one embryonal rhabdomyosarcoma) also showing LOH in the SUFU region.]. 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:16294371;
    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:NP703959.RA9FIm6WeOmPMbWHB_-ueVAQHncngKgnOSSxm5VbPJnpg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}