Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_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." NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_assertion evidence source_evidence_literature NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_assertion SIO_000772 23297193 NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_assertion wasDerivedFrom befree-2016 NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_assertion wasGeneratedBy ECO_0000203 NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1041587.RAi89pkwtk8jdp01rtGtfxCSJI_gWBqfsl4psUnk0-aeY130_provenance.