Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_assertion description "[The cysteine to tyrosine substitution in the NC1 domain of the alpha5 (IV) collagen chain in this family leads to a mild form of Alport syndrome, including absence of extra-renal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_assertion evidence source_evidence_literature NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_assertion SIO_000772 17277342 NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_assertion wasDerivedFrom lhgdn-20090331 NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_assertion wasGeneratedBy ECO_0000203 NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215073.RAlY0rlswWbanmtXOtpS7fhtSqL6zx5c0OIwc8dmR7X6E130_provenance.