Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_assertion description "[Coding SNPs in TLR3 (rs3775291) and TLR7 (rs179008) showed association with AMD in one group (P = 0.01 and P = 0.02, respectively) before correction for multiple testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_assertion evidence source_evidence_literature NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_assertion SIO_000772 18385087 NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_assertion wasDerivedFrom befree-20140225 NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_assertion wasGeneratedBy ECO_0000203 NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP869732.RAUJUPHS0LqbUjmaTO3c4QIT3ETlzv0BjZ6N37oeaoZpk130_provenance.