Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_assertion> ?p ?o ?g. }
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- NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_assertion type Assertion NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_head.
- NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_assertion wasGeneratedBy ECO_0000218 NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_provenance.
- NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_assertion wasDerivedFrom ctd_human-2016 NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_provenance.
- NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_assertion SIO_000772 22961002 NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_provenance.
- NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_assertion evidence source_evidence_curated NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_provenance.
- NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_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." NP31797.RA07TC1z2iAU5-YgMSMrffCpChYGGWWCvZx2cEdgR_8dE130_provenance.