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- source_evidence_literature type ECO_0000212 NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_assertion description "[Clinical findings are different in 9q deletions and duplications including PTCH1, notably concerning the predisposition to benign and malignant tumors reported in the Gorlin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_assertion evidence source_evidence_literature NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_assertion SIO_000772 24486987 NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_assertion wasDerivedFrom befree-2016 NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_assertion wasGeneratedBy ECO_0000203 NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1151171.RADLeDkrvO-Phj6lk9PYMoMgGx7D6t76HDeuMib4v_0cg130_provenance.