@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4> .
@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:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_head {
  this: np:hasAssertion dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_assertion;
    np:hasProvenance dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_provenance;
    np:hasPublicationInfo dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_assertion a np:Assertion .
  
  dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_provenance a np:Provenance .
  
  dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0949059 a ncit:C7057 .
  
  dgn-gda:DGN8ac7d5c35f6f418103181c253f89dd52 sio:SIO_000628 miriam-gene:4595, lld:C0949059;
    a sio:SIO_001121 .
}

dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_provenance {
  dgn-np:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_assertion dcterms:description
      "[The present study investigated germline mutations of the MYH gene among patients with 10 to 99 adenomatous colorectal polyps and familial adenomatous polyposis (FAP) without adenomatous polyposis coli (APC) germline mutations in Korea.]. 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:17703316;
    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:NP348597.RApm_jsCHt_UNnSRLYAsfP8CECJ7MPEpmTMQTN7S5bbg4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:24+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" .
}