@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU> .
@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:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_head {
  this: np:hasAssertion dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_assertion ;
    np:hasProvenance dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_provenance ;
    np:hasPublicationInfo dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_assertion a np:Assertion .
  dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_provenance a np:Provenance .
  dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_assertion {
  miriam-gene:2264 a ncit:C16612 .
  lld:C0024623 a ncit:C7057 .
  dgn-gda:DGNf7a48af403451325e9ba3c5606668218 sio:SIO_000628 miriam-gene:2264 , lld:C0024623 ;
    a sio:SIO_001121 .
}
dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_provenance {
  dgn-np:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_assertion dcterms:description "[Although we observed no correlation between the FGFR4 Gly388Arg polymorphism and clinicopathological parameters or survival in the total cohort of GC patients, the presence of the Arg388 allele was associated with shorter survival time in patients with GC if the tumor was small (log rank χ(2) = 5.449, P = 0.020), well differentiated (log rank χ(2) = 12.798, P = 0.000), T1 or T2 stage (log rank χ(2) = 4.745, P = 0.029), without lymph node involvement (log rank χ(2) = 6.647, P= 0.010), and at an early clinical stage (log rank χ(2) = 4.615, P = 0.032).]. 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:23901234 ;
    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:NP393931.RA25JzLLnnZpbmiYCoZ4nvJI5kTqrH0ROj_LN9Eww0FkU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:54+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" .
}