Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_assertion description "[Both substitution c.214+242C > T in IL1RN and novel deletion c.2558+149_2558+203del54 in SLC4A11 were observed significantly more frequently in family members with KTCN (P = 0.004525 and P = 0.00761, respectively), suggesting involvement of these two genes in KTCN etiology in the studied family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_assertion evidence source_evidence_literature NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_assertion SIO_000772 23462747 NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_assertion wasDerivedFrom befree-20140225 NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_assertion wasGeneratedBy ECO_0000203 NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241567.RA6MwPEvSNO8bjZYxj2GOR59FF0mmYDa5aqy2YzAwYcas130_provenance.