@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw> .
@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:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_head {
  this: np:hasAssertion dgn-np:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_assertion;
    np:hasProvenance dgn-np:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_provenance;
    np:hasPublicationInfo dgn-np:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_publicationInfo;
    a np:Nanopublication .
  
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      np:PublicationInfo .
}

dgn-np:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_assertion {
  miriam-gene:2158 a ncit:C16612 .
  
  lld:C0917713 a ncit:C7057 .
  
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dgn-np:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_provenance {
  dgn-np:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_assertion dcterms:description
      "[This article describes the assay to detect truncated proteins for the APC gene, which can also be applied to other disease causing genetic alterations which commonly lead to truncations such in HNPCC, von Hippel-Lindau, osteogenesis imperfecta, retinoblastoma, BCRAI, beta-thalassemia, hemophilia B, Duchenene and Becker muscular dystrophy.]. 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:11876475;
    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:NP233242.RACtE4vXjvTryBq2mepfzLIQrXbmXZRRCwkYSJM-Gu1vw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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