Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_assertion> ?p ?o ?g. }
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- NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_assertion type Assertion NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_head.
- NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_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." NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_provenance.
- NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_assertion evidence source_evidence_literature NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_provenance.
- NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_assertion SIO_000772 23297193 NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_provenance.
- NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_assertion wasDerivedFrom befree-20140225 NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_provenance.
- NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_assertion wasGeneratedBy ECO_0000203 NP898133.RAkF8G3WC3xvuxjjmo8LAX9gKxRz5odc3I5DSgA3tr1U8130_provenance.