Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_assertion type Assertion NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_head.
- NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_assertion wasGeneratedBy ECO_0000203 NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_provenance.
- NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_assertion wasDerivedFrom befree-20140225 NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_provenance.
- NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_assertion SIO_000772 11576738 NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_provenance.
- NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_assertion evidence source_evidence_literature NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_provenance.
- NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_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." NP369503.RABsKSgqll4-CHQaB8t4bpcHlmfRf3Sj8M83Pt72i4bR0130_provenance.