Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_assertion description "[We describe 2 patients whose clinical features resembled those of multiple system atrophy of the cerebellar subtype (MSA-C) but without ocular motor apraxia and hypoalbuminemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_assertion evidence source_evidence_literature NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_assertion SIO_000772 17049295 NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_assertion wasDerivedFrom befree-2016 NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_assertion wasGeneratedBy ECO_0000203 NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.
- befree-2016 importedOn "2016-02-19" NP575019.RAifm4DgVdMsAcfU4qA8gniC_dvUQfhwC4NXM82abu5qM130_provenance.