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- NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_assertion type Assertion NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_head.
- NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_assertion wasGeneratedBy ECO_0000203 NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_provenance.
- NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_assertion wasDerivedFrom befree-2016 NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_provenance.
- NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_assertion SIO_000772 9633819 NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_provenance.
- NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_assertion evidence source_evidence_literature NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_provenance.
- NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_assertion description "[The associated genetic defects characterized revealed compound heterozygosity for a splice defect leading to skipping of exon 8, due to a G-->A transition at position -1 of the exon 8 splice donor site, and a point mutation leading to a Hisl08Pro change (CAT-->CCT) in two patients (siblings) with mild CESD phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1397736.RAq1s-Kl2x711yEbHtsOu395DwxrMdQeU001x27N60OAI130_provenance.