Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_assertion description "[A novel MPZ mutation in Charcot-Marie-Tooth disease type 1B with focally folded myelin and multiple entrapment neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_assertion evidence source_evidence_literature NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_assertion SIO_000772 21940171 NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_assertion wasDerivedFrom befree-20150227 NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_assertion wasGeneratedBy ECO_0000203 NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568370.RA_i-Wwf6JTS20Ps1-BK_n7-hiT3dwd8WyCq2bJliLKaY130_provenance.