Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_assertion description "[Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_assertion evidence source_evidence_literature NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_assertion SIO_000772 10802646 NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_assertion wasDerivedFrom befree-2016 NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_assertion wasGeneratedBy ECO_0000203 NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.
- befree-2016 importedOn "2016-02-19" NP283244.RAWyqG21LqLf5mwb4kxvMMAHDu2cV-zwoNmTAlscBS-mc130_provenance.