Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1323494.RAoiH-ElyKOOtfyCdbv3vHJyq-mS-NKQeBSlbVLOp3Q-U130_provenance.
- 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.