Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_assertion> ?p ?o ?g. }
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- NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_assertion type Assertion NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_head.
- NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_assertion description "[A 2-year-old boy with manifestations of the fragile X syndrome was found to have a cytogenetically visible deletion of Xq27-q28 including deletion of FMR-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.
- NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_assertion evidence source_evidence_literature NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.
- NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_assertion SIO_000772 7942990 NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.
- NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_assertion wasDerivedFrom befree-2016 NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.
- NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_assertion wasGeneratedBy ECO_0000203 NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.