Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_assertion description "[Only few studies have so far been performed in large groups of hereditary spastic paraplegia (HSP) patients to determine the frequency of SPG7 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_assertion evidence source_evidence_literature NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_assertion SIO_000772 18200586 NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_assertion wasDerivedFrom befree-20140225 NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_assertion wasGeneratedBy ECO_0000203 NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_provenance.