Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_assertion description "[The full FMR-1 mutation is known to cause the fragile X syndrome [Fra(X)], but variable expression in females, including normal to deficient intellect, may be related to random X-inactivation (lyonization).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_assertion evidence source_evidence_literature NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_assertion SIO_000772 7943030 NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_assertion wasDerivedFrom befree-2016 NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_assertion wasGeneratedBy ECO_0000203 NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327690.RAGsLmXUYuX_UMFWM5O6zF4fw585q9AjeK1c3GWFWxVaI130_provenance.