@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_head {
  this: np:hasAssertion dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion;
    np:hasProvenance dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_provenance;
    np:hasPublicationInfo dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion a np:Assertion .
  
  dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_provenance a np:Provenance .
  
  dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion {
  miriam-gene:28471 a ncit:C16612 .
  
  lld:C0206664 a ncit:C7057 .
  
  dgn-gda:DGN3a80350ad4d9d8f9280f6567af9f9b89 sio:SIO_000628 miriam-gene:28471, lld:C0206664;
    a sio:SIO_001121 .
}

dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_provenance {
  dgn-np:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_assertion dcterms:description
      "[We examined eight human germ cell cancer lines (GCCLs) for cytogenetic abnormalities and found an isochromosome 12p, i(12p), marker in all seven male nonseminoma GCCLs, but not in the single female teratocarcinoma cell line.]. 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:2183156;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP891235.RAofSN5JpOlwMdt00ztq0vpKc6O2T0bn8QgvNzRWwT6Kw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:43+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}