@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_head { this: np:hasAssertion dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_assertion; np:hasProvenance dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_provenance; np:hasPublicationInfo dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_publicationInfo; a np:Nanopublication . dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_assertion a np:Assertion . dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_provenance a np:Provenance . dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_publicationInfo a np:PublicationInfo . } dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_assertion { miriam-gene:55536 a ncit:C16612 . lld:C0027051 a ncit:C7057 . dgn-gda:DGNddaf407169fa21a5fb7790141db1cbe7 sio:SIO_000628 miriam-gene:55536, lld:C0027051; a sio:SIO_001121 . } dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_provenance { dgn-np:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_assertion dcterms:description "[After having confirmed that the at-risk C allele of rs1333049 was associated with index ACS in the UK and Belgian populations, we found that the rs1333049 at-risk C allele was significantly and independently associated with recurrent MI [age- and gender-adjusted hazard ratio (HR) 1.48, CI = 1.00-2.19, P = 0.048; and multivariable-adjusted HR 1.47, CI = 0.99-2.18; P = 0.053] and with recurrent MI or cardiac death (age- and gender-adjusted HR 1.58, CI = 1.00-2.48; P = 0.045; and multivariable adjusted HR 1.49, CI = 1.03-1.98; P = 0.028) within 6 months after an index ACS.]. 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:20231156; 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:NP709322.RAhXhO064TOWoysQClwS5MXb-__Cs7_cO5njWMRbuCVQ4130_publicationInfo { this: dcterms:created "2014-10-02T12:39:11+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }