Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_assertion description "[Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_assertion evidence source_evidence_curated NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_assertion SIO_000772 22405088 NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_assertion wasDerivedFrom uniprot-2016 NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_assertion wasGeneratedBy ECO_0000218 NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6996.RA2Uqzbp6YKv6Dvhkqu2vFb3nEQ5E0Yq-4iv2Pwbbt4-U130_provenance.