Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_assertion evidence source_evidence_literature NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_assertion SIO_000772 14530412 NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_assertion wasDerivedFrom befree-20150227 NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_assertion wasGeneratedBy ECO_0000203 NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.