Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_assertion description "[We report a case of a novel splice site mutation in the short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) gene associated with hyperinsulinism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_assertion evidence source_evidence_literature NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_assertion SIO_000772 15870679 NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_assertion wasDerivedFrom befree-20140225 NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_assertion wasGeneratedBy ECO_0000203 NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP273895.RAvMuthwK34b64I3BUaHMX8HuUNCi1qeLOPXN_rw2KmjI130_provenance.