Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP932859.RA0RgfuHtjc7nBz8uYAGR8S71TkeRzBmM8KTCSQDUmZQc130_provenance.