Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_assertion description "[NADH-diaphorase and cytochrome b5 reductase activities of platelets and leucocytes, as well as erythrocytes, were found to be deficient in a patient with hereditary methaemoglobinaemia associated with moderate mental retardation and non-progressive neurological disturbance, in which hyperactive reflexes and involuntary movements were notable.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_assertion evidence source_evidence_literature NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_assertion SIO_000772 6896729 NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_assertion wasDerivedFrom befree-20150227 NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_assertion wasGeneratedBy ECO_0000203 NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP354601.RAXIpaGKovWJn2N50LvzeXLwAzFf5LEbBCCNIsH8bm6HI130_provenance.