Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_assertion> ?p ?o ?g. }
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- NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_assertion type Assertion NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_head.
- NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_assertion wasGeneratedBy ECO_0000203 NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_assertion wasDerivedFrom befree-2016 NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_assertion SIO_000772 7840347 NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_assertion evidence source_evidence_literature NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_assertion description "[Over the past 3 years, reports of DNA alteration in myotonic dystrophy, fragile X syndrome (types A and E), Kennedy's disease, Huntington's disease, spinocerebellar ataxia type 1, and dentatorubral-pallidoluysian atrophy have identified a new class of human mutation, referred to as trinucleotide repeat amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.