Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion> ?p ?o ?g. }
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- NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion type Assertion NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_head.
- NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_provenance.
- NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion evidence source_evidence_literature NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_provenance.
- NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion SIO_000772 7585014 NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_provenance.
- NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion wasDerivedFrom befree-2016 NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_provenance.
- NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_assertion wasGeneratedBy ECO_0000203 NP1313711.RAnLW83w2ma0BL1VB4L7vjf5uVFGunrR9jsco2ppnuGj4130_provenance.