Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_assertion description "[The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_assertion evidence source_evidence_curated NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_assertion SIO_000772 10732799 NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_assertion wasDerivedFrom uniprot-20130724 NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_assertion wasGeneratedBy ECO_0000218 NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2437.RAaCpQ3fCbiQokMoWD5RL9G_H0cAKM5B60PASunsATj6s130_provenance.