Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_assertion description "[Another novel spastin mutation was found in a patient with a rapidly progressive spinal and bulbar UMN syndrome that progressed to amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_assertion evidence source_evidence_literature NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_assertion SIO_000772 16240363 NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_assertion wasDerivedFrom befree-20140225 NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_assertion wasGeneratedBy ECO_0000203 NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP911383.RAgtv5GLI07IHrL5FX1Jvy-KuCzFzgIn5w0XFhXYpNlKk130_provenance.