Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion> ?p ?o ?g. }
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- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion type Assertion NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_head.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion wasGeneratedBy ECO_0000203 NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion wasDerivedFrom befree-20150227 NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion SIO_000772 11576738 NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_assertion evidence source_evidence_literature NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.
- NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_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." NP616921.RAFBcZ6p6_7imy1gpaTb6wXUHuHeLAMQbCniiy276Vi80130_provenance.