Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_assertion description "[Mutations in myotubularin, amphiphysin 2 (BIN1), and dynamin 2 lead to different forms of centronuclear myopathy, while mutations in myotubularin-related proteins cause Charcot-Marie-Tooth neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_assertion evidence source_evidence_literature NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_assertion SIO_000772 22496665 NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_assertion wasDerivedFrom befree-20140225 NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_assertion wasGeneratedBy ECO_0000203 NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP171523.RAv39n9w6EdYQSROHm7e_0ebIpT0K79D4KfTb2tVSVXlw130_provenance.