Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1192681.RANAGxxdQR9sKnlmqBOHHdiAooKoMXvRcqKGA15K-Wyho130_provenance.