@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA> .
@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:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_head {
  this: np:hasAssertion dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_assertion;
    np:hasProvenance dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_provenance;
    np:hasPublicationInfo dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_assertion a np:Assertion .
  
  dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_provenance a np:Provenance .
  
  dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_assertion {
  miriam-gene:3949 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN8cec87e1d905094f9ea520e5b9a9e478 sio:SIO_000628 miriam-gene:3949, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_provenance {
  dgn-np:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_assertion dcterms:description
      "[Some of these rearrangements, such as those involving the MLL locus in leukemia and the LDL receptor in familial hypercholesterolemia, represent recurrent mutations that have independently arisen multiple times in human populations.]. 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:17157332;
    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:NP583373.RATIQltkhMdwkcdCmuU6QAEaugW_uKRqGCmefo5imnntA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:09+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" .
}