@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0> .
@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:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_head {
  this: np:hasAssertion dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_assertion ;
    np:hasProvenance dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_provenance ;
    np:hasPublicationInfo dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_assertion a np:Assertion .
  dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_provenance a np:Provenance .
  dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  lld:C0220620 a ncit:C7057 .
  dgn-gda:DGN150d66c0bd14cff474a9a98f4c60633a sio:SIO_000628 miriam-gene:4436 , lld:C0220620 ;
    a sio:SIO_001121 .
}
dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_provenance {
  dgn-np:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_assertion dcterms:description "[We investigated expression of the two most commonly mutated MMR genes, MSH2 and MLH1, in sporadic testicular germ cell tumor (GCT) in order to: (1) determine the expression pattern of MSH2 and MLH1 proteins in normal seminiferous tubules and histologically distinct GCT subtypes, (2) correlate MMR gene expression with genetic instability in GCT and (3) develop a panel of molecular markers that can identify genetically distinct subsets of GCT for prognostic assessment.]. 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:15467433 ;
    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:NP497643.RAvbiv-qNrMrYcZXNtSyMAMEEnCrDatsDU_Q25LTImYm0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:57+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> ;
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}