Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_assertion description "[Mutations in COQ2 in familial and sporadic multiple-system atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_assertion evidence source_evidence_curated NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_assertion SIO_000772 23758206 NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_assertion wasDerivedFrom uniprot-2016 NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_assertion wasGeneratedBy ECO_0000218 NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7542.RAUndVdW16-z6uhM-s3zbANtczk3m54QfBALJ3ueaYPwU130_provenance.