Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion> ?p ?o ?g. }
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- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion type Assertion NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_head.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion wasGeneratedBy ECO_0000218 NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion wasDerivedFrom uniprot-2016 NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion SIO_000772 22961002 NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_assertion evidence source_evidence_curated NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.
- NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_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." NP7207.RA7CCxmh2O0DMThPpuGEQWM2UtGKDuf8gq2L1-jMk8m88130_provenance.