Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion> ?p ?o ?g. }
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- NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion type Assertion NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_head.
- NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_provenance.
- NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion evidence source_evidence_literature NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_provenance.
- NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion SIO_000772 8162055 NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_provenance.
- NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion wasDerivedFrom befree-20150227 NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_provenance.
- NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion wasGeneratedBy ECO_0000203 NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_provenance.