Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_assertion> ?p ?o ?g. }
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- NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_assertion type Assertion NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_head.
- NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_assertion wasGeneratedBy ECO_0000203 NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_provenance.
- NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_assertion wasDerivedFrom befree-20140225 NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_provenance.
- NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_assertion SIO_000772 11576738 NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_provenance.
- NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_assertion evidence source_evidence_literature NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_provenance.
- NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_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." NP415654.RA2fq01roNSWMmpKXjgnqVqxRD4d3NUdP2aseWQZAR1wg130_provenance.