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- NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_assertion type Assertion NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_head.
- NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_assertion description "[Subsequent studies, however, found that UBQLN2 mutations were rare, and the pathogenicity of SIGMAR1 mutation in FTD and/or motor neuron disease was controversial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_provenance.
- NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_assertion evidence source_evidence_literature NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_provenance.
- NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_assertion SIO_000772 24684794 NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_provenance.
- NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_assertion wasDerivedFrom befree-2016 NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_provenance.
- NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_assertion wasGeneratedBy ECO_0000203 NP1168889.RAvQzuQcYVR4nptT_z5ggJFqn8kkqSmd2pp0_e5qCMHlM130_provenance.