Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_assertion description "[This study supports the recently hypothesized involvement of the ABC7 gene in XLSA/A and highlights a protein structure region of importance to this syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_assertion evidence source_evidence_curated NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_assertion SIO_000772 11843825 NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_assertion wasDerivedFrom uniprot-2016 NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_assertion wasGeneratedBy ECO_0000218 NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1875.RABsYT3gOPgLkwNLhU3DXwIeGZOdoyQ2xRYQNyublDgUc130_provenance.