Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_assertion> ?p ?o ?g. }
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- NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_assertion type Assertion NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_head.
- NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_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." NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_provenance.
- NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_assertion evidence source_evidence_literature NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_provenance.
- NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_assertion SIO_000772 23236003 NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_provenance.
- NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_assertion wasDerivedFrom befree-20150227 NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_provenance.
- NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_assertion wasGeneratedBy ECO_0000203 NP408694.RAZ8FYQT4SZWpCk91b7dIouJ2rjk4Ip_1hqiI4WB82k04130_provenance.