Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_assertion description "[FRAXE mental retardation, a recently identified rare genetic condition, is due to a mutation of the FMR2 gene, located at Xq28 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_assertion evidence source_evidence_literature NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_assertion SIO_000772 10964075 NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_assertion wasDerivedFrom befree-20140225 NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_assertion wasGeneratedBy ECO_0000203 NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_provenance.