Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_assertion> ?p ?o ?g. }
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- NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_assertion type Assertion NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_head.
- NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_assertion description "[Fragile X syndrome (FXS) is caused by a full mutation expansion (>200 CGG repeats) in the FMR1 gene that results in a deficiency of the fragile X mental retardation protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.
- NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_assertion evidence source_evidence_literature NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.
- NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_assertion SIO_000772 16685180 NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.
- NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_assertion wasDerivedFrom befree-20140225 NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.
- NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_assertion wasGeneratedBy ECO_0000203 NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.