Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion description "[ARX mutation testing should be undertaken in children aged less than 1 year with Ohtahara syndrome and a movement disorder, and in infants with unexplained neurodegeneration, progressive white matter loss, and cortical atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion evidence source_evidence_literature NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion SIO_000772 19747203 NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion wasDerivedFrom befree-20150227 NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_assertion wasGeneratedBy ECO_0000203 NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP835514.RAp0YKz5Gf6YEfBXk3NbmuP3AgnHkOfgEGoAJXp79EO5g130_provenance.