Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_assertion description "[Three genes responsible for hereditary motor and sensory neuropathy type I (HMSNI) or CMT1 have been identified: peripheral myelin protein 22 (PMP22) and myelin protein zero (MPZ) for the autosomal dominant form and connexin 32 (Cx32) for the X-linked dominant variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_assertion evidence source_evidence_literature NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_assertion SIO_000772 10975746 NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_assertion wasDerivedFrom befree-20140225 NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_assertion wasGeneratedBy ECO_0000203 NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.
- befree-20140225 importedOn "2014-02-25" NP806841.RADX462guOji1aOceNmVFJqR1owWJelMwLTK5Wr1KtYug130_provenance.