Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_assertion description "[Multiple carboxylase deficiency (MCD, MIM:253270) is a common organic aciduria and caused by deficiency of either biotinidase or holocarboxylase synthetase (HLCS; EC 6.3.4.10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_assertion evidence source_evidence_literature NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_assertion SIO_000772 12633764 NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_assertion wasDerivedFrom befree-20140225 NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_assertion wasGeneratedBy ECO_0000203 NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP261096.RANHq1YBU91NJCrjx0g59T6Y_FNTToadbGHmfISl83fqM130_provenance.