Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_assertion> ?p ?o ?g. }
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- NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_assertion type Assertion NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_head.
- NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_assertion wasGeneratedBy ECO_0000203 NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_provenance.
- NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_assertion wasDerivedFrom befree-20140225 NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_provenance.
- NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_assertion SIO_000772 11576738 NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_provenance.
- NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_assertion evidence source_evidence_literature NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_provenance.
- NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_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." NP924193.RA_GPF-dQ0YuturHv0QOd7WHPiju18bVgTbVCQA_1iHS4130_provenance.