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- NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_assertion type Assertion NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_head.
- NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_assertion wasGeneratedBy ECO_0000203 NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_provenance.
- NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_assertion wasDerivedFrom befree-2016 NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_provenance.
- NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_assertion SIO_000772 17030535 NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_provenance.
- NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_assertion evidence source_evidence_literature NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_provenance.
- NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_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." NP573569.RAGzLNerkkOwjcq-oLfwtCyYnEqgabIoRJ9e9RAGnZ2sQ130_provenance.