Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion> ?p ?o ?g. }
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- NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion type Assertion NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_head.
- NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion description "[The objective of this study was to identify the frequency of REEP1 mutations in both autosomal dominant HSP (ADHSP) and sporadic spastic paraparesis (SSP) cases and to analyse the genotype/phenotype correlation of mutations so far described in REEP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_provenance.
- NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion evidence source_evidence_literature NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_provenance.
- NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion SIO_000772 19034539 NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_provenance.
- NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion wasDerivedFrom gad-20130706 NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_provenance.
- NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_assertion wasGeneratedBy ECO_0000203 NP76708.RAWS7gVGmuFfp79_L8yk92ACl-_DEUQH5cngJ2Ofu-_90130_provenance.