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- source_evidence_literature type ECO_0000212 NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_assertion evidence source_evidence_literature NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_assertion SIO_000772 21829228 NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_assertion wasDerivedFrom befree-20140225 NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_assertion wasGeneratedBy ECO_0000203 NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP388590.RA0z_2CY9RqWEbNlzfIZoUPOxHh_cwvUyx-k8b7JNJBH8130_provenance.