Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_assertion description "[The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_assertion evidence source_evidence_curated NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_assertion SIO_000772 9158144 NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_assertion wasDerivedFrom uniprot-2016 NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_assertion wasGeneratedBy ECO_0000218 NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9385.RA6-2_qt4neyvbxi8h0kvQqVOkbaQbKCsAE0THMR3tv4A130_provenance.