@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ> .
@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:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_head {
  this: np:hasAssertion dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_assertion;
    np:hasProvenance dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_provenance;
    np:hasPublicationInfo dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_assertion a np:Assertion .
  
  dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_provenance a np:Provenance .
  
  dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_assertion {
  miriam-gene:1869 a ncit:C16612 .
  
  lld:C2931876 a ncit:C7057 .
  
  dgn-gda:DGN88565d2652af2ce285613f9a9fe00b55 sio:SIO_000628 miriam-gene:1869, lld:C2931876;
    a sio:SIO_001121 .
}

dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_provenance {
  dgn-np:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_assertion dcterms:description
      "[MEN2A and MEN2B have recently been mapped within the centromeric region closely linked to RBP3 and D10S15 (which are located inside the deletion) and cosegregate with HSCR in at least two different pedigrees.]. 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:8467706;
    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:NP346030.RAy3sOr0IX281sZ3ZSwZ44GdBDx4wEe8qtsMKpQJBRpdQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:23+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" .
}