Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_assertion description "[In the haplotype analysis, htC-T-G (P=0.003) and htA-C-G (P=0.032) in ADORA1 and htA-T in ADORA2 (P=0.013) were significantly associated with AIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_assertion evidence source_evidence_literature NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_assertion SIO_000772 19019667 NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_assertion wasDerivedFrom gad-20150221 NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_assertion wasGeneratedBy ECO_0000203 NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP134120.RArToCntygnccRwH9wLTMvXfOkvedXg5O9VBuB9jw25xM130_provenance.