Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1327677.RALkQZDgmVl5RgC0iAtGmrVtdSB-h6MPl-JeC7w18uyK4130_provenance.