Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_assertion description "[CMT2A is an axonal autosomal dominant CMT type which in most cases is characterized by early onset and rather severe course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_assertion evidence source_evidence_literature NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_assertion SIO_000772 25847151 NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_assertion wasDerivedFrom befree-2016 NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_assertion wasGeneratedBy ECO_0000203 NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.
- befree-2016 importedOn "2016-02-19" NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.