Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_assertion description "[Severe erythrocyte adenylate kinase deficiency due to homozygous A-->G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_assertion evidence source_evidence_curated NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_assertion SIO_000772 9432020 NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_assertion wasDerivedFrom uniprot-20130724 NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_assertion wasGeneratedBy ECO_0000218 NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP281.RAi3Mjub7HvZU_XeIqWw0CLs0fFqrec1fbttno4x6AAC0130_provenance.