Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_assertion description "[Recently, several point mutations of the human gas3/PMP22 gene have been associated with Charcot-Marie-Tooth type 1A (CMT1A), a common hereditary demyelinating neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_assertion evidence source_evidence_literature NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_assertion SIO_000772 7649472 NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_assertion wasDerivedFrom befree-20140225 NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_assertion wasGeneratedBy ECO_0000203 NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP317080.RA6ukKK31mOaydQh2eEr1DwpYFj4wfelCWUEIZ1UAmdWo130_provenance.