Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_assertion description "[X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_assertion evidence source_evidence_literature NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_assertion SIO_000772 12177367 NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_assertion wasDerivedFrom befree-20150227 NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_assertion wasGeneratedBy ECO_0000203 NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP850002.RAdmgOQyXjrFf85F-DWp7S7IqGoB6v6245j7aZVJaadzA130_provenance.