Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_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." NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_assertion evidence source_evidence_literature NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_assertion SIO_000772 6896729 NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_assertion wasDerivedFrom befree-20150227 NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_assertion wasGeneratedBy ECO_0000203 NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP353748.RAqkXsYVk2zdcRy9DJ9H3Xq-dsK1x8QNvfj57b3VP81zI130_provenance.