@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w> .
@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:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_head {
  this: np:hasAssertion dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_assertion;
    np:hasProvenance dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_provenance;
    np:hasPublicationInfo dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_assertion a np:Assertion .
  
  dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_provenance a np:Provenance .
  
  dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C0238339 a ncit:C7057 .
  
  dgn-gda:DGN5629760e8dbaac75465ee015477551b5 sio:SIO_000628 miriam-gene:4292, lld:C0238339;
    a sio:SIO_001122 .
}

dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_provenance {
  dgn-np:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_assertion dcterms:description
      "[Second, the samples from Finnish hereditary prostate cancer (HPC) families were used for the screening of MLH1 mutations which produced twelve MLH1 sequence variants including two missense mutations, I219V, as in the PRCA-colon cancer patient, and V647M.]. 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:16963262;
    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:NP558358.RAUD0C-KPmgykU-8BIZSX5ZLyMW3xuZ-nEpP66rzc7S3w130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:12+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" .
}