Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_assertion description "[Dysfunction of Cdk5 has been implicated in a number of neurological disorders and neurodegenerative diseases including Alzheimer's disease, amyotrophic lateral sclerosis, Niemann-Pick type C disease, and ischemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_assertion evidence source_evidence_literature NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_assertion SIO_000772 21740229 NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_assertion wasDerivedFrom befree-20140225 NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_assertion wasGeneratedBy ECO_0000203 NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889635.RARrX-_EeL41QpYTNLHn0C33OcqkomV6UgUU-1pIEaqfU130_provenance.