Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_assertion type Assertion NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_head.
- NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_assertion description "[Here, we use untargeted metabolomics combined with a genetic mouse model to determine that the poorly characterized serine hydrolase ?/?-hydrolase domain-containing (ABHD)12, mutations in which cause the human neurodegenerative disorder PHARC (polyneuropathy, hearing loss, ataxia, retinosis pigmentosa, and cataract), is a principal lysophosphatidylserine (LPS) lipase in the mammalian brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_provenance.
- NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_assertion evidence source_evidence_literature NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_provenance.
- NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_assertion SIO_000772 23297193 NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_provenance.
- NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_assertion wasDerivedFrom befree-20140225 NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_provenance.
- NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_assertion wasGeneratedBy ECO_0000203 NP588924.RAKWn6Au0niukZTa3hSplWnmf_j28MpiOpqVz1nh5vfH8130_provenance.