@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk> .
@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:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_head {
  this: np:hasAssertion dgn-np:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_assertion ;
    np:hasProvenance dgn-np:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_provenance ;
    np:hasPublicationInfo dgn-np:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_provenance a np:Provenance .
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}
dgn-np:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_assertion {
  miriam-gene:4851 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGN95763950cc34ad0a35f099c31b880f54 sio:SIO_000628 miriam-gene:4851 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_provenance {
  dgn-np:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_assertion dcterms:description "[To see whether NOTCH1 mutation occurs in other malignancies, we analyzed NOTCH1 for the detection of somatic mutations in 334 malignancies, including 48 lung, 48 breast, 48 colorectal and 48 gastric carcinomas, and 142 acute leukemias (105 acute myelogenous leukemias, 32 B-ALLs and 4 T-ALLs) by single-strand conformation polymorphism assay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP541016.RAHEmgNN-Ud2Gm0bURWCoJhEZqZn_0h-UhZebiD4OoHFk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:26+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
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    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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