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- source_evidence_literature type ECO_0000212 NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_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." NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_assertion evidence source_evidence_literature NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_assertion SIO_000772 21829228 NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_assertion wasDerivedFrom befree-2016 NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_assertion wasGeneratedBy ECO_0000203 NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.
- befree-2016 importedOn "2016-02-19" NP915868.RABEb_KzVVgTtQGI0xdixhWe5o3VWekMfWZkvQgfhVZHg130_provenance.