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- source_evidence_literature type ECO_0000212 NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_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." NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_assertion evidence source_evidence_literature NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_assertion SIO_000772 17388790 NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_assertion wasDerivedFrom befree-20150227 NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_assertion wasGeneratedBy ECO_0000203 NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978367.RAIp1LMjoM0-17S2ptRRqyolt9mow3gvuI1bxnRsfiZZo130_provenance.