Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_assertion description "[The 35delG, 167delT, and 235delC mutations in the Cx26 gene are the main cause for sporadic nonsyndromic hearing loss (NSHL) in many populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_assertion evidence source_evidence_literature NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_assertion SIO_000772 18554165 NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_assertion wasDerivedFrom befree-2016 NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_assertion wasGeneratedBy ECO_0000203 NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.
- befree-2016 importedOn "2016-02-19" NP676665.RA6W0nFSjlDwF8YX3VupO4D3R6W4m93iq7d6P_Gacew4w130_provenance.