Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_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." NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_assertion evidence source_evidence_curated NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_assertion SIO_000772 9158144 NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_assertion wasDerivedFrom uniprot-20150221 NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_assertion wasGeneratedBy ECO_0000218 NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP1505.RAjz-TCcbPocVOmjWg8sUKtBQ-3S1ksrxoJUxh1v3ixNY130_provenance.