Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion description "[The new SPG7 gene mutation leads to a novel complicated autosomal recessive hereditary spastic paraparesis phenotype that widens the spectrum of different brain systems that are optionally affected in hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion evidence source_evidence_literature NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion SIO_000772 17646629 NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion wasDerivedFrom lhgdn-20090331 NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_assertion wasGeneratedBy ECO_0000203 NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP141634.RAs1wPgdvehpKszVZN2G-Tl670wLOfAiOsWliPIggQl28130_provenance.