Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_assertion description "[Genotypes that cause disease at the phenylalanine hydroxylase (PAH) gene and galactose-1-phosphate uridyltransferase (GALT) gene in a group of 101 hyperphenylalaninaemic and 77 patients with classic galactosaemia were established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_assertion evidence source_evidence_literature NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_assertion SIO_000772 11678552 NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_assertion wasDerivedFrom befree-2016 NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_assertion wasGeneratedBy ECO_0000203 NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP334285.RA3JiwxepZu5Qee7CS5z5rWBcEbpmIWEjjCzmYuhWa38Q130_provenance.