@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo> .
@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:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_head {
   this: np:hasAssertion dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_assertion ;
    np:hasProvenance dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_provenance ;
    np:hasPublicationInfo dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_assertion a np:Assertion .
  dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_provenance a np:Provenance .
  dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_assertion {
   miriam-gene:4810 a ncit:C16612 .
  lld:C0007137 a ncit:C7057 .
  dgn-gda:DGNf56ec0f557ccf0940cdd556742dd11e7 sio:SIO_000628 miriam-gene:4810 , lld:C0007137 ;
    a sio:SIO_001121 .
}
dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_provenance {
   dgn-np:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_assertion dcterms:description "[We evaluated the effect of MDM2 SNP309 and its interaction with the p53 Arg72Pro polymorphism on pigmentary phenotypes and skin cancer risk in a nested case-control study within the Nurses' Health Study (NHS) among 219 melanoma cases, 286 squamous cell carcinoma (SCC) cases, 300 basal cell carcinoma (BCC) cases, and 873 controls, and among controls from other studies.]. 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:18814047 ;
    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:NP756216.RA_F0SpPkxCbxljdzrBbCmPrlF1YbKTjoVkZ2Q7vkwGoo130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:38+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> ;
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}