Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_assertion> ?p ?o ?g. }
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- NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_assertion type Assertion NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_head.
- NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_assertion description "[Fragile X syndrome is primarily due to a CGG repeat expansion found in the FMR1 X-linked gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_provenance.
- NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_assertion evidence source_evidence_literature NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_provenance.
- NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_assertion SIO_000772 17295053 NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_provenance.
- NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_assertion wasDerivedFrom befree-2016 NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_provenance.
- NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_assertion wasGeneratedBy ECO_0000203 NP593382.RAAs9wiWyiRMcXFp227B4FW6YrlJeeklhbKdDKyHTLX4Y130_provenance.