Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_assertion description "[In a case-control sample that has shown the well established associations between AMD and variants in CFH, CFB and C3 there was absence of association with SNPs in CFP, CD46, CD55 and CD59.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_assertion evidence source_evidence_literature NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_assertion SIO_000772 22024702 NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_assertion wasDerivedFrom befree-2016 NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_assertion wasGeneratedBy ECO_0000203 NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.
- befree-2016 importedOn "2016-02-19" NP933405.RA2WaMrIQF7unok3vZdN8XfEp6yjnTpAPe0SwPQLvC1PY130_provenance.