@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE> .
@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:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_head {
  this: np:hasAssertion dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_assertion;
    np:hasProvenance dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_provenance;
    np:hasPublicationInfo dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_assertion a np:Assertion .
  
  dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_provenance a np:Provenance .
  
  dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_assertion {
  miriam-gene:4484 a ncit:C16612 .
  
  lld:C0007137 a ncit:C7057 .
  
  dgn-gda:DGN8643f63076706657393c23b04351a2d2 sio:SIO_000628 miriam-gene:4484, lld:C0007137;
    a sio:SIO_001121 .
}

dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_provenance {
  dgn-np:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_assertion dcterms:description
      "[Familial predisposition to basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) of the skin are apparent in the autosomal dominant syndromes naevoid basal cell carcinoma syndrome (NBCCS) and multiple self-healing squamous epitheliomata (MSSE) 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:8688329;
    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:NP827250.RA98E1TMGc0eqfkUvBaSnDRUX4pxuQ07g-wvFlAMVNHcE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:26+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" .
}