@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8> .
@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:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_head {
  this: np:hasAssertion dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_assertion ;
    np:hasProvenance dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_provenance ;
    np:hasPublicationInfo dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_assertion a np:Assertion .
  dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_provenance a np:Provenance .
  dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_assertion {
  miriam-gene:23600 a ncit:C16612 .
  lld:C0027086 a ncit:C7057 .
  dgn-gda:DGN2bd746184ee64a9eb7f7019a774eb3f5 sio:SIO_000628 miriam-gene:23600 , lld:C0027086 ;
    a sio:SIO_001121 .
}
dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_provenance {
  dgn-np:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_assertion dcterms:description "[To determine the spectrum and nature of the aberrations in uterine myomas in Japanese patients, we systematically examined the tumors of 45 patients for all possible types of gene fusions involving HMGIC, by means of 3'-rapid amplification of cDNA ends (RACE) and reverse transcriptase-polymerase chain reaction (RT-PCR) experiments.]. 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:11450849 ;
    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:NP694023.RA7McT9EC1qMJ3OSd6oefAEg5zU-qy0mgI2X-O7zbE-a8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:02+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" .
}