@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:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_head { this: np:hasAssertion dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_assertion; np:hasProvenance dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_provenance; np:hasPublicationInfo dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_publicationInfo; a np:Nanopublication . dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_assertion a np:Assertion . dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_provenance a np:Provenance . dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_publicationInfo a np:PublicationInfo . } dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_assertion { miriam-gene:9993 a ncit:C16612 . lld:C0340100 a ncit:C7057 . dgn-gda:DGN7da16bd973a6df647b132a5bc45f502d sio:SIO_000628 miriam-gene:9993, lld:C0340100; a sio:SIO_001121 . } dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_provenance { dgn-np:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_assertion dcterms:description "[Allele frequencies of three loci in SP-A1 and one in SP-A2 were significantly different between LAN HAPE patients (SP-A1 C1101T: C allele, 36.4% and T allele, 63.6%; SP-A1 T3192C: T allele, 61.1% and C allele, 38.9%; SP-A1 T3234C: T allele, 61.1% and C allele, 38.9%; and SP-A2 A3265C: A allele, 21.4% and C allele, 78.6%) and LAN control subjects (SP-A1 C1101T: C allele, 8.3% and T allele, 91.7%; SP-A1 T3192C: T allele, 15% and C allele, 85%; SP-A1 T3234C: T allele, 15% and C allele, 85%; and SP-A2 A3265C: A allele, 37.5% and C allele, 62.5%) [C1101T odds ratio [OR], 6.3 with 95% confidence interval (CI), 2.8 to 14.3; T3192C OR, 8.9 with 95% CI, 4.5 to 17.6; T3234C OR, 8.9 with 95% CI, 4.5 to 17.6; and A3265C OR, 2.2 with 95% CI, 1.2 to 4.1 (p < or = 0.01)].]. 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:16162765; 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:NP174903.RAWm6XWHrohyfl0CKha63VhbttP9B-Mi16f9om3znadTI130_publicationInfo { this: dcterms:created "2014-10-02T12:33:34+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" . }