Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_assertion> ?p ?o ?g. }
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- NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_assertion type Assertion NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_head.
- NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_assertion description "[The fragile X syndrome is a mutation-driven developmental disorder caused by a repetition over 200 times of the CGG trinucleotide situated in the 5'-untranslated region of the fragile X mental retardation 1 gene (FMR1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_provenance.
- NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_assertion evidence source_evidence_literature NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_provenance.
- NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_assertion SIO_000772 23236003 NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_provenance.
- NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_assertion wasDerivedFrom befree-20140225 NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_provenance.
- NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_assertion wasGeneratedBy ECO_0000203 NP474916.RABww-vvBtK6B2_qsJKRgs98LuGf-rZsOYJyal-DB4y8g130_provenance.