Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_assertion> ?p ?o ?g. }
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- NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_assertion type Assertion NP436855.RAkVVV_GB0mnfJdsQAIy_v4h2RPxhcI1VvXrd76-i7m1I130_head.
- 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.