Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_assertion description "[Highly penetrant, non-synonymous, or insertion-deletion mutations in TERF1 and TERF2 were not identified and therefore are not likely to be major genetic risk factors for the development of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_assertion evidence source_evidence_literature NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_assertion SIO_000772 16647572 NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_assertion wasDerivedFrom gad-20130706 NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_assertion wasGeneratedBy ECO_0000203 NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66681.RAmw3GH4ox3SLj8TMCWafuy_3YoCu4Oa3TNRlfsswvcoc130_provenance.