@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs> .
@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:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_head {
  this: np:hasAssertion dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_assertion;
    np:hasProvenance dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_provenance;
    np:hasPublicationInfo dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_assertion a np:Assertion .
  
  dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_provenance a np:Provenance .
  
  dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_assertion {
  miriam-gene:1243 a ncit:C16612 .
  
  lld:C0205748 a ncit:C7057 .
  
  dgn-gda:DGN0a88619e253f48ee5abd4cc5141be6a6 sio:SIO_000628 miriam-gene:1243, lld:C0205748;
    a sio:SIO_001121 .
}

dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_provenance {
  dgn-np:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_assertion dcterms:description
      "[Although the first English-language report of melanoma in 1820 contained a description of a melanoma-prone family, seminal studies by investigators at the National Cancer Institute and the University of Pennsylvania identified dysplastic nevi (DN) as an important melanoma precursor, suggested an autosomal dominant mode of inheritance for both melanoma and DN, and proposed that a melanoma-susceptibility gene (CMM1) was located on chromosome 1p36.]. 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:9146691;
    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:NP828895.RAEwixckr0pInv2oiRTMInGhRyoxTPHVUBR7qw7sMd7xs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:27+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" .
}