Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_assertion wasGeneratedBy ECO_0000218 NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_assertion wasDerivedFrom uniprot-20150221 NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_assertion SIO_000772 12357336 NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_assertion evidence source_evidence_curated NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.
- NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_assertion description "[DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162.RAaYNSoO-jx5poNodE0jkC8V2BFjMEv17HgLzE5auFISo130_provenance.