Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_assertion description "[Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_assertion evidence source_evidence_literature NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_assertion SIO_000772 6896729 NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_assertion wasDerivedFrom befree-20140225 NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_assertion wasGeneratedBy ECO_0000203 NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP239116.RAYCUrMLnzaf2WrY4_AR-9sP66Zpz2NfvWDYbbRnkufY0130_provenance.