@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE> .
@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:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_head {
  this: np:hasAssertion dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_assertion;
    np:hasProvenance dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_provenance;
    np:hasPublicationInfo dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_assertion a np:Assertion .
  
  dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_provenance a np:Provenance .
  
  dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_assertion {
  miriam-gene:4627 a ncit:C16612 .
  
  lld:C0398641 a ncit:C7057 .
  
  dgn-gda:DGNd25053205266a31772924cfc6b83e261 sio:SIO_000628 miriam-gene:4627, lld:C0398641;
    a sio:SIO_001121 .
}

dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_provenance {
  dgn-np:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_assertion dcterms:description
      "[The clinical features of EPTS and the chromosomal localization of the respective gene in the same region as MYH9 suggest that this disorder is allelic with the other giant platelet disorders.]. 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:11935325;
    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:NP154109.RA4bF8rUBF-7N6TDOfsB6DhKvT4JM6g5RlPF1v2cYHzLE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}