Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_assertion> ?p ?o ?g. }
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- NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_assertion type Assertion NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_head.
- NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_assertion wasGeneratedBy ECO_0000203 NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_provenance.
- NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_assertion wasDerivedFrom befree-20140225 NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_provenance.
- NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_assertion SIO_000772 11576738 NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_provenance.
- NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_assertion evidence source_evidence_literature NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_provenance.
- NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_assertion description "[Myotonic dystrophy (DM), Huntington's disease (HD) and Fragile X syndrome (FRAXA) are three monogenic disease which are caused by so-called dynamic mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898701.RAyiGxsIi7icUYG65JumwqHbnWVtlCmd86Owp2M-ZTVh0130_provenance.