Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_assertion> ?p ?o ?g. }
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- NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_assertion type Assertion NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_head.
- NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_assertion wasGeneratedBy ECO_0000203 NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_provenance.
- NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_assertion wasDerivedFrom befree-2016 NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_provenance.
- NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_assertion SIO_000772 11576738 NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_provenance.
- NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_assertion evidence source_evidence_literature NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_provenance.
- NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_assertion description "[PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331335.RARZaHDx7E6VIAZJKW78LP4Myxh9USt7I8MNnTM3EPiQk130_provenance.