Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_assertion description "[We searched for SLC35D1 mutations in five families with SBD and 15 patients with other SSDD group diseases, including achodrogenesis type 1A, spondylometaphyseal dysplasia Sedaghatian type and fibrochondrogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_assertion evidence source_evidence_literature NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_assertion SIO_000772 19508970 NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_assertion wasDerivedFrom befree-2016 NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_assertion wasGeneratedBy ECO_0000203 NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.
- befree-2016 importedOn "2016-02-19" NP744122.RA0G3CEPCpgedCL-qTvTeyiQ2H86T53vjFHYKDaRZh0Lo130_provenance.