@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY> .
@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:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_head {
  this: np:hasAssertion dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_assertion ;
    np:hasProvenance dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_provenance ;
    np:hasPublicationInfo dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_assertion a np:Assertion .
  dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_provenance a np:Provenance .
  dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_assertion {
  miriam-gene:727837 a ncit:C16612 .
  lld:C0178874 a ncit:C7057 .
  dgn-gda:DGNbceebabd941492e428bd1fbddc248a10 sio:SIO_000628 miriam-gene:727837 , lld:C0178874 ;
    a sio:SIO_001121 .
}
dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_provenance {
  dgn-np:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_assertion dcterms:description "[We conclude that the expression pattern of OCT2, SSX2-4, and SAGE1 supports the origin of SS from spermatogonia and provides new evidence for heterogeneity of this tumour, potentially linked either to the cellular origin of SS or to partial differentiation during tumour progression, including a hitherto unknown OCT2-positive variant of the tumour likely derived from A(dark) spermatogonia.]. 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:21706474 ;
    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:NP629288.RAHIOL1sF-AtkgpX6Vux2XwwKxY_K52Kq7IVupETKSVFY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:19+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" .
}