Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- befree-2016 importedOn "2016-02-19" NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_assertion wasGeneratedBy ECO_0000203 NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_assertion wasDerivedFrom befree-2016 NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_assertion SIO_000772 19651702 NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_assertion evidence source_evidence_literature NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.
- NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755134.RAsixUhsWAyDDE2RG91fxF1pgbyc7lLRVseadOWtWKCJ8130_provenance.