Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_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." NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_assertion evidence source_evidence_curated NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_assertion SIO_000772 10732799 NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_assertion wasDerivedFrom uniprot-20150221 NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_assertion wasGeneratedBy ECO_0000218 NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3724.RAN_8qSzhW-PGKbExp7w7RYhRwzR-Fwb6F4xxJm5uuSys130_provenance.