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- source_evidence_literature type ECO_0000212 NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_assertion description "[Previously, a genome scan of 98 families affected by SLI was completed by the SLI Consortium, resulting in the identification of two quantitative trait loci (QTL) on chromosomes 16q (SLI1) and 19q (SLI2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_assertion evidence source_evidence_literature NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_assertion SIO_000772 17388790 NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_assertion wasDerivedFrom befree-20140225 NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_assertion wasGeneratedBy ECO_0000203 NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209715.RAxRHaIFFG-wKLH2uaMSlcx4W3mXB7BM63MbqmigmEcy4130_provenance.