Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_assertion type Assertion NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_head.
- NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_assertion description "[Fragile X syndrome (FXS) is caused by CGG repeat expansion that leads to FMR1 silencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_provenance.
- NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_assertion evidence source_evidence_literature NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_provenance.
- NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_assertion SIO_000772 25179629 NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_provenance.
- NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_assertion wasDerivedFrom befree-2016 NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_provenance.
- NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_assertion wasGeneratedBy ECO_0000203 NP1216065.RAJAVtqXyzbmRJ8yzJ06xQ5i3Qxg5pTqhMzORilEChP2E130_provenance.