Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_assertion description "[In a similar study, we also failed to sustain an association between C4BP polymorphisms and predisposition to age-related macular degeneration, another disorder which is associated strongly with polymorphisms in factor H, and is thought to involve alternative pathway dysregulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_assertion evidence source_evidence_literature NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_assertion SIO_000772 19076829 NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_assertion wasDerivedFrom befree-20140225 NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_assertion wasGeneratedBy ECO_0000203 NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP516919.RAG1Q0Fa88jjIDRCDL4EeOnUFYFNBTqae2gOms-SD_yPA130_provenance.