Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_assertion description "[Variants in the factor H gene (CFH, also known as HF1), which encodes a major inhibitor of the alternative complement pathway, are associated with the risk for developing AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_assertion evidence source_evidence_literature NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_assertion SIO_000772 16518403 NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_assertion wasDerivedFrom befree-2016 NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_assertion wasGeneratedBy ECO_0000203 NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.
- befree-2016 importedOn "2016-02-19" NP538827.RA_rHfbFF-0kDS4Hdu2aPT--Bbx5erb9CcCmBixA-dbww130_provenance.