@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_head {
  this: np:hasAssertion dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_assertion;
    np:hasProvenance dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_provenance;
    np:hasPublicationInfo dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_assertion a np:Assertion .
  
  dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_provenance a np:Provenance .
  
  dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0085390 a ncit:C7057 .
  
  dgn-gda:DGNe4d949a2047b5864b6a0f8da0e43e496 sio:SIO_000628 miriam-gene:7157, lld:C0085390;
    a sio:SIO_001121 .
}

dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_provenance {
  dgn-np:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_assertion dcterms:description
      "[The frequency of germ line p53 mutations can now be examined in additional families with LFS, and in other cancer patients and families with clinical features that might be attributed to the mutation.]. 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:1978757;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP766071.RANy339g-8pNvbg20bUkmc0uwl2RHSsi7Z1TqSw8drmII130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:32+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}