Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_assertion> ?p ?o ?g. }
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- NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_assertion type Assertion NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_head.
- NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_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." NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_provenance.
- NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_assertion evidence source_evidence_literature NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_provenance.
- NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_assertion SIO_000772 24934289 NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_provenance.
- NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_assertion wasDerivedFrom befree-20150227 NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_provenance.
- NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_assertion wasGeneratedBy ECO_0000203 NP991488.RAiM1S4qJDpALMIna98cGfP8uZwD5GpEtlKGkaBr7uKdw130_provenance.