Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_assertion description "[The genotypes of the polymorphisms in the known AMD susceptibility loci (CFH, AMRS2, HTRA1, VEGFA, and KDR) were determined, and association between their frequencies and the changes in the BCVA and the CSMT were evaluated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_assertion evidence source_evidence_literature NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_assertion SIO_000772 23559864 NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_assertion wasDerivedFrom befree-2016 NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_assertion wasGeneratedBy ECO_0000203 NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1066788.RAMK1H-sxCRTTv2NFCsk0QPIQNvQ-_TaQpsJVsPVeyTWk130_provenance.