Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_assertion description "[In the haplotype analysis, ht[C-T-G] (P=0.003) and ht[A-C-G] (P=0.032) in ADORA1 and ht[A-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." NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_assertion evidence source_evidence_literature NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_assertion SIO_000772 19019667 NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_assertion wasDerivedFrom befree-20140225 NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_assertion wasGeneratedBy ECO_0000203 NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP373040.RApJGTuKWLSfa18kmCiFGqYeGiSk3QcmyMZb0a6wFe4kQ130_provenance.