@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE> .
@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:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_head {
   this: np:hasAssertion dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_assertion ;
    np:hasProvenance dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_provenance ;
    np:hasPublicationInfo dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_assertion a np:Assertion .
  dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_provenance a np:Provenance .
  dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_assertion {
   miriam-gene:2064 a ncit:C16612 .
  lld:C1261473 a ncit:C7057 .
  dgn-gda:DGN806bffe062ab1c7aff1da1eb6aa23339 sio:SIO_000628 miriam-gene:2064 , lld:C1261473 ;
    a sio:SIO_001121 .
}
dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_provenance {
   dgn-np:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_assertion dcterms:description "[Except for a few tests such as assessment of HER2/neu for gene amplification in breast cancer, detection of clonality in hematopoietic neoplasms, and specific chromosomal translocations in the former and in the diagnosis of soft tissue sarcoma, most of the molecular tests using FNAB specimens are currently investigational.]. 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:17342764 ;
    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:NP793007.RAc0XPeDEzxxmEKO6mTKMbf3lliWWIfPZIO2kZGmaKRpE130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:07+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" .
}