Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_assertion> ?p ?o ?g. }
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- NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_assertion type Assertion NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_head.
- NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_assertion wasGeneratedBy ECO_0000203 NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_provenance.
- NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_assertion wasDerivedFrom befree-2016 NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_provenance.
- NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_assertion SIO_000772 21926154 NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_provenance.
- NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_assertion evidence source_evidence_literature NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_provenance.
- NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_assertion description "[Presently, guidelines for FMR1 genetic testing includes early menopause, congenital intellectual disability, autism spectrum disorder, tremor or ataxia, and a family history of FXTAS or fragile X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924459.RA6lhpAm7XYUfFAGWiYf07fBBkR_SZYUOwmLJw5kHWn1A130_provenance.