Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion> ?p ?o ?g. }
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- NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion type Assertion NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_head.
- NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion description "[The identification of a hexanucleotide repeat expansion in the C9ORF72 gene as the cause of chromosome 9-linked frontotemporal dementia and motor neuron disease offers the opportunity for greater understanding of the relationship between these disorders and other clinical forms of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_provenance.
- NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion evidence source_evidence_literature NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_provenance.
- NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion SIO_000772 22300873 NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_provenance.
- NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion wasDerivedFrom befree-2016 NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_provenance.
- NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_assertion wasGeneratedBy ECO_0000203 NP958158.RAwrwqXbVQHJEpMTa6gNCg8YfK5-g2qvNgvdjxD704n_c130_provenance.