Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_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." NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_assertion evidence source_evidence_literature NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_assertion SIO_000772 7726217 NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_assertion wasDerivedFrom befree-20140225 NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_assertion wasGeneratedBy ECO_0000203 NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP460127.RAbIyPN_nZrzDqIfhrDxLIC8D_d2vvzVZh3eVZXW6Ptfc130_provenance.