Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion description "[Our findings document that patients carrying these SCAD gene variations may develop clinically relevant SCAD deficiency, and that patients with even mild ethylmalonic aciduria should be tested for these variations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion evidence source_evidence_curated NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion SIO_000772 11134486 NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion wasDerivedFrom uniprot-20150221 NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_assertion wasGeneratedBy ECO_0000218 NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1743.RAZJ2iQE0T19qnF1vY3k2b9vPwI_vzA4aQ4fxDfzVAiyg130_provenance.