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- source_evidence_literature type ECO_0000212 NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_assertion description "[The lack of any strong association between C4 variants and RA overall makes it unlikely that the association between RA and genes within the MHS represents a direct effect of variants within the C4A or C4B loci themselves.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_assertion evidence source_evidence_literature NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_assertion SIO_000772 2711369 NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_assertion wasDerivedFrom befree-20150227 NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_assertion wasGeneratedBy ECO_0000203 NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP676842.RAtovMGubt4NiKIa51TllFdQZVoFfF2LfhmHASjn5xrhc130_provenance.