Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_assertion type Assertion NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_head.
- NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_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." NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.
- NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_assertion evidence source_evidence_literature NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.
- NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_assertion SIO_000772 17566607 NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.
- NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_assertion wasDerivedFrom befree-20150227 NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.
- NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_assertion wasGeneratedBy ECO_0000203 NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.