@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0> .
@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/v4.0.0/void/> .

dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_head {
  this: np:hasAssertion dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_assertion;
    np:hasProvenance dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_provenance;
    np:hasPublicationInfo dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_assertion a np:Assertion .
  
  dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_provenance a np:Provenance .
  
  dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C0238462 a ncit:C7057 .
  
  dgn-gda:DGNa4e32ace11c67c0f54e7db8a09f0a0cc sio:SIO_000628 miriam-gene:4221, lld:C0238462;
    a sio:SIO_001121 .
}

dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_provenance {
  dgn-np:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_assertion dcterms:description
      "[Extension of the screening program can now be anticipated for other inherited forms of MTC, such as familial MTC without pheochromocytoma or other endocrinological tumor syndromes such as MEN1 for which the locus has also recently been mapped.]. 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:2575577;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1269869.RAgbklZZnJJIXuF0JKegRO6JdPCauJIRS9_yCxDyk58u0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:22+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: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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}