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- source_evidence_literature type ECO_0000212 NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_assertion description "[Renal function was normal except for 1 patient with a MLL2 mutation diagnosed in the first days of life and severe renal disease due to unilateral renal agenesia and controlateral severe hypoplasia that progressed to the terminal stage at age 2 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_assertion evidence source_evidence_literature NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_assertion SIO_000772 23535010 NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_assertion wasDerivedFrom befree-20150227 NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_assertion wasGeneratedBy ECO_0000203 NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.
- befree-20150227 importedOn "2015-02-27" NP789740.RAZZ4DXI1xY__EehiXW_JqrsHwoRg1HVl72lqY9n4Y_to130_provenance.