Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_assertion description "[Re-analysis in the original DFNB 17 family and additional data from a second unrelated consanguineous family with congenital deafness found to map to the interval, limited the area of shared homozygosity-by-descent (HBD) to approximately 4 megabase (Mb) between markers D7S2453 and D7S525.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_assertion evidence source_evidence_literature NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_assertion SIO_000772 15293785 NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_assertion wasDerivedFrom befree-20140225 NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_assertion wasGeneratedBy ECO_0000203 NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP211955.RARzm4rGeAFM4-YeXx3YFnYtJ1aIA_W9M8imeFUmDsVmE130_provenance.