Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_assertion> ?p ?o ?g. }
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- NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_assertion type Assertion NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_head.
- NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_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." NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_provenance.
- NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_assertion evidence source_evidence_literature NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_provenance.
- NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_assertion SIO_000772 7585014 NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_provenance.
- NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_assertion wasDerivedFrom befree-20150227 NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_provenance.
- NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_assertion wasGeneratedBy ECO_0000203 NP412591.RAy8H05dcmtlp_uX4WRhfV3Azlpjb_dmQJ__74z-DJ1Ko130_provenance.