Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_assertion description "[Dejerine-Sottas disease (DSD), also called hereditary motor and sensory neuropathy type III (HMSNIII), is a severe, infantile-onset demyelinating polyneuropathy syndrome that may be associated with point mutations in either the PMP22 gene or the P0 gene and shares considerable clinical and pathological features with CMT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_assertion evidence source_evidence_literature NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_assertion SIO_000772 10219749 NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_assertion wasDerivedFrom befree-2016 NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_assertion wasGeneratedBy ECO_0000203 NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.
- befree-2016 importedOn "2016-02-19" NP251186.RAyEs3euaZEH8Xqzs2m8Mpy1sh9ejyBj19NF1D4cb0fH8130_provenance.