@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:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_head { this: np:hasAssertion dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_assertion; np:hasProvenance dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_provenance; np:hasPublicationInfo dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_publicationInfo; a np:Nanopublication . dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_assertion a np:Assertion . dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_provenance a np:Provenance . dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_publicationInfo a np:PublicationInfo . } dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_assertion { miriam-gene:4541 a ncit:C16612 . lld:C0011265 a ncit:C7057 . dgn-gda:DGN8b0c83ca0183b535ed2fc3ff06f75ef1 sio:SIO_000628 miriam-gene:4541, lld:C0011265; a sio:SIO_001121 . } dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_provenance { dgn-np:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_assertion dcterms:description "[Participants from haplogroup T had a statistically significant increased risk of developing dementia (OR = 1.86, 95% CI = 1.23, 2.82, p = 0.0008) and haplogroup J participants experienced a statistically significant 8-year decline in 3MS (β = -0.14, 95% CI = -0.27, -0.03, p = 0.0006), both compared with common haplogroup H. The m.15244A>G, p.G166G, CytB variant was associated with a significant decline in DSST score (β = -0.58, 95% CI -0.89, -0.28, p = 0.00019) and the m.14178T>C, p.I166V, ND6 variant was associated with a significant decline in 3MS score (β = -0.87, 95% CI -1.31, -3.86, p = 0.00012).]. 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:22785396; 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:NP248907.RAUo8wF3jN5LJgKPgnQqg9WTuQYe-v8vlaJlEkFghRW3E130_publicationInfo { this: dcterms:created "2014-10-02T12:34:19+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" . }