Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_assertion wasGeneratedBy ECO_0000218 NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_assertion wasDerivedFrom uniprot-2016 NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_assertion SIO_000772 8490648 NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_assertion evidence source_evidence_curated NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.
- NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_assertion description "[Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8925.RAApiy1J2i0HJXIS6QFBUiSx5ZYvxAD4uSvNMXJE8IlcA130_provenance.