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- NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_assertion type Assertion NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_head.
- NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_assertion wasGeneratedBy ECO_0000203 NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_provenance.
- NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_assertion wasDerivedFrom befree-2016 NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_provenance.
- NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_assertion SIO_000772 7888141 NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_provenance.
- NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_assertion evidence source_evidence_literature NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_provenance.
- NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_assertion description "[The findings in the present family illustrate that the typical characteristics of the fragile X syndrome can be caused by other types of mutations involving the FMR1 than the highly expanded stretches of CGG repeats in the 5' noncoding region of the FMR1 gene, coinciding with abnormal methylation patterns in that area as present in the vast majority of individuals with the fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1325058.RAi_3Mg1x2u8Tbk7IBjtDQHxitvOvwCFani5A4a6rc1SA130_provenance.