Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_assertion> ?p ?o ?g. }
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- NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_assertion type Assertion NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_head.
- NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_assertion wasGeneratedBy ECO_0000218 NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_provenance.
- NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_assertion wasDerivedFrom ctd_human-20150221 NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_provenance.
- NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_assertion SIO_000772 22961002 NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_provenance.
- NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_assertion evidence source_evidence_curated NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_provenance.
- NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_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." NP17008.RADriYP8uoT2VCsgZqaRHVwtPNqz45UuqlMy9i8BJG6QM130_provenance.