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- NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_assertion type Assertion NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_head.
- NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_assertion wasGeneratedBy ECO_0000203 NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_provenance.
- NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_assertion wasDerivedFrom befree-20150227 NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_provenance.
- NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_assertion SIO_000772 17030535 NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_provenance.
- NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_assertion evidence source_evidence_literature NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_provenance.
- NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_assertion description "[These findings suggest that the insR352 PSEN1 is not pathogenic, and the IVS1+1G-->A mutation in PGRN causes FTDP associated with FTLD-U pathology and represents a new class of neurodegenerative disease--the 'hypoprogranulinopathies'.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650805.RA8RFXOC1nCCDVtIf-qS5eitvjS3KyboeSo-sWH430mVk130_provenance.