@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY> .
@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:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_head {
  this: np:hasAssertion dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_assertion ;
    np:hasProvenance dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_provenance ;
    np:hasPublicationInfo dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_assertion a np:Assertion .
  dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_provenance a np:Provenance .
  dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_assertion {
  miriam-gene:7039 a ncit:C16612 .
  lld:C0025202 a ncit:C7057 .
  dgn-gda:DGN8f8528d9e550c1e846963acd2f40ecbf sio:SIO_000628 miriam-gene:7039 , lld:C0025202 ;
    a sio:SIO_001121 .
}
dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_provenance {
  dgn-np:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_assertion dcterms:description "[To determine whether atypical, compared to benign nevi, from patients with a clinical history of malignant melanoma reveal molecular changes, we analyzed these lesions for the expression of two growth factors (basic fibroblast growth factor and transforming growth factor alpha), their receptors (fibroblast growth factor receptor-1 and epidermal growth factor receptor), and two cell adhesion molecules (MUC18 and alpha v beta 3 integrin), all of which are expressed in primary and metastatic melanomas.]. 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:8959342 ;
    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:NP768447.RAvK7rEAnblXddw3djaJWmITuWtj3i5HLv7HC0_8jMKuY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:45+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" .
}