Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_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." NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_assertion evidence source_evidence_curated NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_assertion SIO_000772 12357336 NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_assertion wasDerivedFrom uniprot-20130724 NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_assertion wasGeneratedBy ECO_0000218 NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP5049.RATuF7DtDA1YpqAUwBDMJaRUklxdQTSmVkYHQdeZMbU2k130_provenance.