Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_assertion evidence source_evidence_literature NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_assertion SIO_000772 23941260 NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_assertion wasDerivedFrom befree-20150227 NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_assertion wasGeneratedBy ECO_0000203 NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP867790.RAvjazLefx583xkXJeggYMB1a_kBtcwd7vjIBAuTalGpg130_provenance.