Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_assertion> ?p ?o ?g. }
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- NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_assertion type Assertion NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_head.
- NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_assertion description "[ALS2 is a causative gene for a juvenile autosomal recessive form of motor neuron diseases (MNDs), including amyotrophic lateral sclerosis 2 (ALS2), juvenile primary lateral sclerosis, and infantile-onset ascending hereditary spastic paralysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.
- NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_assertion evidence source_evidence_literature NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.
- NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_assertion SIO_000772 17566607 NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.
- NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_assertion wasDerivedFrom befree-20150227 NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.
- NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_assertion wasGeneratedBy ECO_0000203 NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.