Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_assertion description "[A novel AMT gene mutation in a newborn with nonketotic hyperglycinemia and early myoclonic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_assertion evidence source_evidence_curated NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_assertion SIO_000772 26371980 NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_assertion wasDerivedFrom uniprot-2016 NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_assertion wasGeneratedBy ECO_0000218 NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP8201.RAj18LcAg4E_oHdW-5atpuKi9vsXB0Ilp48nKwev0KYsU130_provenance.