@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY> .
@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:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_head {
  this: np:hasAssertion dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion ;
    np:hasProvenance dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_provenance ;
    np:hasPublicationInfo dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion a np:Assertion .
  dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_provenance a np:Provenance .
  dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0037579 a ncit:C7057 .
  dgn-gda:DGN5e11cdcce59ebdc9f6cebd9d6bfd0ab3 sio:SIO_000628 miriam-gene:7157 , lld:C0037579 ;
    a sio:SIO_001121 .
}
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_provenance {
  dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion dcterms:description "[The p53 tumor suppressor gene is a possible candidate underlying the syndrome because (a) mutations in the p53 gene are ubiquitous in human cancer, including colon carcinoma and gliomas, and (b) somatic or germ line mutations of the p53 tumor suppressor gene cause the Li-Fraumeni syndrome, which is characterized by the association of breast and soft tissue tumors.]. 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:8439970 ;
    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:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:09+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" .
}