Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_assertion description "[This report emphasizes concurrently that ABCC6 may be a relevant candidate gene in some cases of GACI with no mutations in the ENPP1 gene, and that GACI may be an atypical and severe end of the vascular phenotype spectrum of PXE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_assertion evidence source_evidence_curated NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_assertion SIO_000772 20034067 NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_assertion wasDerivedFrom uniprot-2016 NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_assertion wasGeneratedBy ECO_0000218 NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6047.RAtWqKxnOUMK8apr6k0UPeALUJxmkt2S3d4OXAWW8Jaoo130_provenance.