@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4> .
@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:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_head {
   this: np:hasAssertion dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_assertion ;
    np:hasProvenance dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_provenance ;
    np:hasPublicationInfo dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_assertion a np:Assertion .
  dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_provenance a np:Provenance .
  dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_assertion {
   miriam-gene:7428 a ncit:C16612 .
  lld:C0017638 a ncit:C7057 .
  dgn-gda:DGN02f986a5826df3733763281f62a8de2b sio:SIO_000628 miriam-gene:7428 , lld:C0017638 ;
    a sio:SIO_001121 .
}
dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_provenance {
   dgn-np:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_assertion dcterms:description "[Non-VHL microsatellites studied for loss of heterozygosity (LOH) are near tumor suppressor genes lost in gliomas, pituitary adenomas, several CNS tumors on 22q, neurofibromatosis 1, and colon carcinomas (13, 2, 2, 1, and 2 markers for each, respectively).]. 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:15343513 ;
    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:NP570221.RAVN2ldfnqYfq9zpkPYZm1Ix0nGrOjOL1L0brgvE_KOH4130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:44+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" .
}