Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion description "[In the field of the peripheral neuropathies we present data on a newly described autosomal recessive Charcot-Marie-Tooth disease (CMT4F) with mutations in the periaxin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion evidence source_evidence_literature NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion SIO_000772 12094560 NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion wasDerivedFrom befree-20140225 NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_assertion wasGeneratedBy ECO_0000203 NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583002.RAzEhSV9X4THe7G1DyPmsIxl4jRjxDPZuEBd9jpKEBKbU130_provenance.