Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_assertion wasGeneratedBy ECO_0000218 NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_assertion wasDerivedFrom uniprot-20130724 NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_assertion SIO_000772 8770875 NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_assertion evidence source_evidence_curated NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_assertion description "[Our findings demonstrate that isolated persistent hypermethioninemia is a marker of MAT I/III deficiency, and that complete lack of MAT I/III activity can lead to neurological abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP3935.RAaHlya54DvU5QshlOfMi3YCkHza3tTGgG_OnAPzz-PAY130_provenance.