Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_assertion description "[We carried out a case-control study to test for association between AMD and single nucleotide polymorphisms (SNPs) spanning the genes encoding complement factor P (CFP, properdin), CD46 (membrane cofactor protein, MCP), CD55 (decay accelerating factor, DAF) and CD59 (protectin).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_assertion evidence source_evidence_literature NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_assertion SIO_000772 22024702 NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_assertion wasDerivedFrom befree-2016 NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_assertion wasGeneratedBy ECO_0000203 NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.
- befree-2016 importedOn "2016-02-19" NP933402.RAKakTsVR_p9ttsH08gMguTgUbi2iaLq0pRETdBhdT6Sc130_provenance.