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- NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_assertion type Assertion NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_head.
- NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_assertion wasGeneratedBy ECO_0000203 NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_provenance.
- NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_assertion wasDerivedFrom befree-2016 NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_provenance.
- NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_assertion SIO_000772 18954413 NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_provenance.
- NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_assertion evidence source_evidence_literature NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_provenance.
- NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_assertion description "[Our aims were to establish how common TUBA1A mutations are in patients with lissencephaly and to contribute to defining the phenotype associated with TUBA1A mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700123.RA9cTf3L743xMm5cRFGm3ZOAMndtdnTtCiwNvRetlHotA130_provenance.