Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_assertion description "[Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_assertion evidence source_evidence_curated NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_assertion SIO_000772 24268659 NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_assertion wasDerivedFrom uniprot-20150221 NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_assertion wasGeneratedBy ECO_0000218 NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP331.RAd8EPb_64SMhvAcTEtC2KyFlrIZ0YwpyF4RI2pAkh9kM130_provenance.