Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_assertion description "[Causative genes have been identified only in four types of lipid storage myopathies (LSMs): SLC22A5 for primary carnitine deficiency (PCD); ETFA, ETFB, and ETFDH for multiple acyl-coenzyme A dehydrogenation deficiency (MADD); PNPLA2 for neutral lipid storage disease with myopathy (NLSDM); and ABHD5 for neutral lipid storage disease with ichthyosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_assertion evidence source_evidence_literature NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_assertion SIO_000772 19208393 NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_assertion wasDerivedFrom gad-20150221 NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_assertion wasGeneratedBy ECO_0000203 NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140749.RAXmUdQpnbLJKFBVrDZZsPNVlOvitZgE1SOz7s9a3Js9I130_provenance.