@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME> .
@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:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_head {
  this: np:hasAssertion dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_assertion;
    np:hasProvenance dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_provenance;
    np:hasPublicationInfo dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_assertion a np:Assertion .
  
  dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_provenance a np:Provenance .
  
  dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_assertion {
  miriam-gene:4088 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGNfa8bb5eec9baa47325e0cd172a9b9fa5 sio:SIO_000628 miriam-gene:4088, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_provenance {
  dgn-np:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_assertion dcterms:description
      "[Losses of 15q and 18q material are frequent in pancreatic carcinomas, and in order to map the extent of 15q and 18q deletions and to investigate further the involvement of SMAD4 and the possible function of SMAD2 and SMAD3 as tumor suppressor genes in pancreatic carcinoma, we performed loss of heterozygosity studies as well as mutation and expression analyses of SMAD4, SMAD2, and SMAD3 in 13 low-passage cell lines from 12 pancreatic carcinoma patients.]. 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:9892110;
    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:NP246903.RAUHED2lG_p9MnAH5WI9BXLWZqQ5ETe8AbuJn7aui7hME130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:18+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" .
}