Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_assertion description "[Charcot-Marie-Tooth disease comprises a heterogeneous group of hereditary neuropathies which fall into two main groups: demyelinating CMT1 with reduced nerve conduction velocity and axonal CMT2 with normal nerve conduction velocity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_assertion evidence source_evidence_literature NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_assertion SIO_000772 14733962 NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_assertion wasDerivedFrom befree-20140225 NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_assertion wasGeneratedBy ECO_0000203 NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP902481.RAqP4Fn8n0vIGX7DATmSRVnGnLWBD5VOGN_7yfXlwizWA130_provenance.