Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion wasGeneratedBy ECO_0000218 NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion wasDerivedFrom uniprot-20150221 NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion SIO_000772 22961002 NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion evidence source_evidence_curated NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.
- NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_assertion description "[Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2744.RADh-KGQFf4FtQWqtNrYBlfsAqfJYgvZpRBeID0dCUTE8130_provenance.