Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_assertion> ?p ?o ?g. }
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- NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_assertion type Assertion NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_head.
- NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_assertion description "[The cytogenetic expression of the folate sensitive fragile site, FRAXE, is due to the expansion of a GCC repeat in proximal Xq28 of the human X chromosome and is associated with a mild form of mental handicap.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_provenance.
- NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_assertion evidence source_evidence_literature NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_provenance.
- NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_assertion SIO_000772 8824884 NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_provenance.
- NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_assertion wasDerivedFrom befree-2016 NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_provenance.
- NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_assertion wasGeneratedBy ECO_0000203 NP1358268.RAXPz8SV21yvz6dXrCrI4Vyp3tZJ9rpzp-IZVw0Z9j3xY130_provenance.