Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_assertion description "[Dynamin 2 (DNM2)-related dominant centronuclear myopathy is usually a mild disorder, but more severe variants have been associated with mutations affecting the pleckstrin homology (PH) domain of the protein, mainly implicated in different forms of Charcot-Marie-Tooth Disease (CMT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_assertion evidence source_evidence_literature NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_assertion SIO_000772 19932620 NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_assertion wasDerivedFrom befree-20140225 NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_assertion wasGeneratedBy ECO_0000203 NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP838223.RAXrS2YGR2AbSP-aAmje-GgFtsWYPoiE2Ys1D51O6fHQA130_provenance.