Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_assertion> ?p ?o ?g. }
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- NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_assertion type Assertion NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_head.
- NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_assertion wasGeneratedBy ECO_0000203 NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_provenance.
- NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_assertion wasDerivedFrom befree-2016 NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_provenance.
- NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_assertion SIO_000772 22961002 NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_provenance.
- NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_assertion evidence source_evidence_literature NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_provenance.
- NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_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." NP1011410.RAlKHsaN56QPJALFJnB9vXyGxSXaa_TSrcD-9dtg7pzeU130_provenance.