@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA> .
@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:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_head {
  this: np:hasAssertion dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_assertion;
    np:hasProvenance dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_provenance;
    np:hasPublicationInfo dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_assertion a np:Assertion .
  
  dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_provenance a np:Provenance .
  
  dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_assertion {
  miriam-gene:4221 a ncit:C16612 .
  
  lld:C0023798 a ncit:C7057 .
  
  dgn-gda:DGNd4c82c4b91a2927ac6aafbee4d981d4c sio:SIO_000628 miriam-gene:4221, lld:C0023798;
    a sio:SIO_001121 .
}

dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_provenance {
  dgn-np:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_assertion dcterms:description
      "[Hereditary predisposition to lipomas is observed in familial multiple lipomatosis (OMIM 151900) and benign cervical lipomatosis (OMIM 151800) and can also be associated with mutations in the MEN1 and PTEN genes (OMIM 131100 and 153480, respectively).]. 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:11571558;
    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:NP780230.RAUsMQiV8sKDREdCPIRuBnI_kbtnDPaeX9uqwidVsd2LA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:52+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" .
}