@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo> .
@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:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_head {
   this: np:hasAssertion dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_assertion ;
    np:hasProvenance dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_provenance ;
    np:hasPublicationInfo dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_assertion a np:Assertion .
  dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_provenance a np:Provenance .
  dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_assertion {
   miriam-gene:7005 a ncit:C16612 .
  lld:C0025202 a ncit:C7057 .
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dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_provenance {
   dgn-np:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_assertion dcterms:description "[We used the genotyping data of 1,115 common single nucleotide polymorphisms (SNPs) in the 12 pathway core genes (i.e., MST1, MST2, SAV1, LATS1, LATS2, MOB1A, MOB1B, YAP1, TEAD1, TEAD2, TEAD3 and TEAD4) from the dataset of our previously published CM genome-wide association study and comprehensively analyzed their associations with CM-specific survival (CSS) in 858 CM patients by using the Kaplan-Meier analyses and Cox proportional hazards regression models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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  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:NP1259010.RAAP4qd3dcSnkRDY1V524bXRmmKQ4-Ukvcq_DU9XdmKKo130_publicationInfo {
   this: dcterms:created "2016-05-13T12:51:17+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}