Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_assertion> ?p ?o ?g. }
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- NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_assertion type Assertion NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_head.
- NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_assertion wasGeneratedBy ECO_0000203 NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_provenance.
- NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_assertion wasDerivedFrom befree-20140225 NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_provenance.
- NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_assertion SIO_000772 19667223 NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_provenance.
- NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_assertion evidence source_evidence_literature NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_provenance.
- NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_assertion description "[In addition, neither the mutation type nor the location of the mutation were found to predict the severity of LIS1-related lissencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP170918.RAA8-X3NgIDafb-ILLOhacgcqUYAxxlHemPG0IBrvxVyU130_provenance.