Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- befree-2016 importedOn "2016-02-19" NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_assertion wasGeneratedBy ECO_0000203 NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_assertion wasDerivedFrom befree-2016 NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_assertion SIO_000772 15148151 NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_assertion evidence source_evidence_literature NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.
- NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_assertion description "[Autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [SCA] 1-SCA8, SCA10-SCA19, SCA21, SCA22, fibroblast growth factor 14 [FGF14]-SCA, and dentatorubral-pallidoluysian atrophy [DRPLA]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP444475.RA5aCSTGDbK546y672lE3A4wOVU8MRgkafCpYp27hmW_U130_provenance.