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- NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_assertion type Assertion NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_head.
- NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_assertion wasGeneratedBy ECO_0000203 NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_provenance.
- NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_assertion wasDerivedFrom befree-20140225 NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_provenance.
- NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_assertion SIO_000772 20220177 NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_provenance.
- NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_assertion evidence source_evidence_literature NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_provenance.
- NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_assertion description "[We identified and validated compound, heterozygous, causative alleles in SH3TC2 (the SH3 domain and tetratricopeptide repeats 2 gene), involving two mutations, in the proband and in family members affected by Charcot-Marie-Tooth disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281591.RApkgM_sePjtm0BGJpySQ7-eX5-skUK49hfjE3_GAzajw130_provenance.