@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY> .
@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:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_head {
  this: np:hasAssertion dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_assertion ;
    np:hasProvenance dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_provenance ;
    np:hasPublicationInfo dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_assertion a np:Assertion .
  dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_provenance a np:Provenance .
  dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_assertion {
  miriam-gene:115761 a ncit:C16612 .
  lld:C0006826 a ncit:C7057 .
  dgn-gda:DGN7c5d2d448bdb100a713b7d60fafd45fb sio:SIO_000628 miriam-gene:115761 , lld:C0006826 ;
    a sio:SIO_001121 .
}
dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_provenance {
  dgn-np:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_assertion dcterms:description "[On the contrary, the ARLTS1-MUT induced significantly lower levels of apoptosis in infected cells and reduced in vivo tumorigenesis only partially, supporting the hypothesis that Trp149Stop polymorphism is retained in the general population and predisposes to cancer because of a reduction, but not full loss, of normal ARLTS1 function.]. 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:17079447 ;
    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:NP706172.RAABW_eHnBwabVP2m4gy6Uv5A15ob_but6fR1ggH9q_EY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:09+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" .
}