Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion wasGeneratedBy ECO_0000203 NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion wasDerivedFrom befree-20140225 NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion SIO_000772 12134148 NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion evidence source_evidence_literature NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_assertion description "[SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.
- befree-20140225 importedOn "2014-02-25" NP742199.RAC3RnH4kgSSm0rla68D3FTQIXIELXaVYRF_zSwv6w944130_provenance.