Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_assertion wasGeneratedBy ECO_0000218 NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_assertion wasDerivedFrom ctd_human-2016 NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_assertion SIO_000772 22961002 NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_assertion evidence source_evidence_curated NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.
- NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_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." NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_provenance.