Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_assertion> ?p ?o ?g. }
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- NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_assertion type Assertion NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_head.
- NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_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." NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_provenance.
- NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_assertion evidence source_evidence_literature NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_provenance.
- NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_assertion SIO_000772 17566607 NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_provenance.
- NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_assertion wasDerivedFrom befree-20140225 NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_provenance.
- NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_assertion wasGeneratedBy ECO_0000203 NP366912.RAst0ndbGpRRuB7jnlMa4lbw4SBFdZ95QMvrm5JTbhJdo130_provenance.