Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_assertion description "[Most (78.3%) of the 23 G6PD deficient neonates who subsequently suffered from neonatal hyperbilirubinemia carried the nt 1376 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_assertion evidence source_evidence_literature NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_assertion SIO_000772 8571933 NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_assertion wasDerivedFrom befree-2016 NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_assertion wasGeneratedBy ECO_0000203 NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1346186.RAZYfOyK7B1pXH1k612ArUErGCLSWhCmMwy17j5kkQQ7I130_provenance.