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- source_evidence_literature type ECO_0000212 NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_assertion description "[Initial linkage studies with color blindness (CB), glucose-6-phosphate dehydrogenase (G6PD) deficiency, and the blood coagulation factor IX (F9) have suggested that a gene for BP illness is located in the Xq27-q28 region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_assertion evidence source_evidence_literature NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_assertion SIO_000772 7726217 NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_assertion wasDerivedFrom befree-20150227 NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_assertion wasGeneratedBy ECO_0000203 NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP415651.RA80eHX1d5emK_lLnYDwPYTRZjsHcjU9Au_LlYRUkCByM130_provenance.