Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_assertion wasGeneratedBy ECO_0000203 NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_assertion wasDerivedFrom befree-2016 NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_assertion SIO_000772 23125284 NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_assertion evidence source_evidence_literature NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.
- NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_assertion description "[A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1026002.RAVx1qvglxcfuZOTNOb0smCxODu3Dc0S4NaCz-l9xSy8c130_provenance.