Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_assertion> ?p ?o ?g. }
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- NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_assertion type Assertion NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_head.
- NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_assertion wasGeneratedBy ECO_0000203 NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_provenance.
- NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_assertion wasDerivedFrom befree-2016 NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_provenance.
- NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_assertion SIO_000772 8825916 NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_provenance.
- NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_assertion evidence source_evidence_literature NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_provenance.
- NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_assertion description "[The identification of the FMR1 gene involved in fragile X syndrome allows testing of the assumption that the fragile X locus is normally subject to X inactivation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1358357.RA9ltvlpiLx_jpf1Frp6th7_MQszATxOU6nF1OS2FaqGc130_provenance.