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- source_evidence_literature type ECO_0000212 NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_assertion description "[Fragile X syndrome, the most common heritable form of cognitive impairment, is caused by epigenetic silencing of the fragile X (FMR1) gene owing to large expansions (>200 repeats) of a non-coding CGG-repeat element.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_assertion evidence source_evidence_literature NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_assertion SIO_000772 23867198 NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_assertion wasDerivedFrom befree-2016 NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_assertion wasGeneratedBy ECO_0000203 NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1094842.RAwdxlBpc14OVCoSyl_EoGpxs7oAc7Al7p6mXekJumqgY130_provenance.