Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_assertion> ?p ?o ?g. }
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- NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_assertion type Assertion NP31796.RAIg1XIoHt9Vb8bmUkqIhnz2lSNC_6iWTpmggjjiMaar4130_head.
- 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.