Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_assertion evidence source_evidence_literature NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_assertion SIO_000772 10982389 NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_assertion wasDerivedFrom befree-20150227 NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_assertion wasGeneratedBy ECO_0000203 NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP662180.RAJ14-aG_SF1cQjo8iR4kBsE1ALBYOPYT0vd7QH7VW2Mc130_provenance.