Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_assertion> ?p ?o ?g. }
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- NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_assertion type Assertion NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_head.
- NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_assertion description "[The observation of a frontotemporal dementia-amyotrophic lateral sclerosis phenotype in a mitochondrial disease led us to analyse CHCHD10 in a cohort of 21 families with pathologically proven frontotemporal dementia-amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.
- NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_assertion evidence source_evidence_literature NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.
- NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_assertion SIO_000772 24934289 NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.
- NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_assertion wasDerivedFrom befree-2016 NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.
- NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_assertion wasGeneratedBy ECO_0000203 NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.