Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_assertion description "[We have investigated the molecular lesions of T-protein deficiency causing typical or atypical nonketotic hyperglycinemia (NKH) in two unrelated pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_assertion evidence source_evidence_curated NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_assertion SIO_000772 8005589 NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_assertion wasDerivedFrom uniprot-20150221 NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_assertion wasGeneratedBy ECO_0000218 NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2701.RAk4tqn-7l4b9fnT9565E8F0dlnTvEiaLAOVqaRoi9vNo130_provenance.