Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_assertion> ?p ?o ?g. }
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- NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_assertion type Assertion NP605327.RAVXy4D1PC_YXIbWXlWOFjiQ-Ucu4oJVquafOWF6XVyjM130_head.
- 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.