@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU> .
@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:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_head {
  this: np:hasAssertion dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_assertion;
    np:hasProvenance dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_provenance;
    np:hasPublicationInfo dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_assertion a np:Assertion .
  
  dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_provenance a np:Provenance .
  
  dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_assertion {
  miriam-gene:1022 a ncit:C16612 .
  
  lld:C0587248 a ncit:C7057 .
  
  dgn-gda:DGN9de4344aaf81f6b5afd5d71959cae5b2 sio:SIO_000628 miriam-gene:1022, lld:C0587248;
    a sio:SIO_001121 .
}

dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_provenance {
  dgn-np:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_assertion dcterms:description
      "[While there is significant phenotypic overlap among syndromes of the Ras/MAPK pathway, individuals with CS are more likely than individuals with CFC syndrome to present with cutaneous papillomas, palmoplantar keratoderma and full eyebrows, and are less likely to present with ulerythema ophryogenes, keratosis pilaris or multiple naevi.]. 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:22098123;
    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:NP699979.RAJReF-IPsViYpX6dhecaYqakKyi3FZYOo7XYSNL4YZuU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:05+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" .
}