Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_assertion> ?p ?o ?g. }
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- NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_assertion type Assertion NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_head.
- NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_assertion wasGeneratedBy ECO_0000203 NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_provenance.
- NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_assertion wasDerivedFrom befree-20140225 NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_provenance.
- NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_assertion SIO_000772 11222639 NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_provenance.
- NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_assertion evidence source_evidence_literature NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_provenance.
- NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_assertion description "[L1 gene mutations are present in humans with the X-linked mental retardation syndrome CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia, hydrocephalus).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705373.RAeQNcd5coYXIhF3w_t9KprEopiUOl4-pIJiP-sj3Le10130_provenance.