Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_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." NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_assertion evidence source_evidence_literature NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_assertion SIO_000772 6896729 NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_assertion wasDerivedFrom befree-2016 NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_assertion wasGeneratedBy ECO_0000203 NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1307230.RAgxVHfXDV5kCMqZAqkYcL_M_QkNfvvTCm07s9G2oABEo130_provenance.