Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion description "[Charcot-Marie-Tooth type 1B (CMT1B) is a demyelinating neuropathy caused by mutations in the myelin protein zero (MPZ) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion evidence source_evidence_literature NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion SIO_000772 21940171 NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion wasDerivedFrom befree-2016 NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_assertion wasGeneratedBy ECO_0000203 NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.
- befree-2016 importedOn "2016-02-19" NP925748.RA0QxpwMn4s5stpDJ02vpqR0QhIoLsyH067JZoTM76mDw130_provenance.