Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP932806.RA7Ucn2dBUwF4gi1H5hzVdN0l3AGfrou9bKFtcewjqapA130_provenance.