Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_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." NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_assertion evidence source_evidence_curated NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_assertion SIO_000772 16518403 NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_assertion wasDerivedFrom ctd_human-20130708 NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_assertion wasGeneratedBy ECO_0000218 NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP11644.RAvKSP2Fffv_FPc0ZxaO8Dd_KmQMRVwjBnplv_iX6RImI130_provenance.