Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_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." NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_assertion evidence source_evidence_literature NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_assertion SIO_000772 14733962 NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_assertion wasDerivedFrom befree-20150227 NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_assertion wasGeneratedBy ECO_0000203 NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP868169.RAmwe1-LE0qz_1tboWw23XsOpFzSeZL9F4yJWxsKIAAQI130_provenance.