Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP231181.RA6j-arlYc-WejQ1zxoplcr05WKUgR-_YzDvVsEZpJlac130_provenance.