Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_assertion description "[Disruptions of the C-terminal domain of SQSTM1 seem to be a leading cause of familial PDB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_assertion evidence source_evidence_curated NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_assertion SIO_000772 14584883 NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_assertion wasDerivedFrom uniprot-20130724 NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_assertion wasGeneratedBy ECO_0000218 NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6363.RAfNYBcNCeWGwcFzN2tvhUG2CcIpAH7oLkQ2XcZxjAnLU130_provenance.