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- source_evidence_literature type ECO_0000212 NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_assertion description "[To examine the association of genetic polymorphisms in this region with chronic kidney disease (CKD; estimated glomerular filtration rate <60 ml/min/1.73 m(2)) in individuals of European ancestry, we examined rs4821480, an MYH9 single-nucleotide polymorphism (SNP) recently identified as associated with kidney disease in African-Americans, in 13 133 participants from the Framingham Heart Study (FHS) and Atherosclerosis Risk in Communities (ARIC) Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_assertion evidence source_evidence_literature NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_assertion SIO_000772 21429915 NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_assertion wasDerivedFrom befree-2016 NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_assertion wasGeneratedBy ECO_0000203 NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.
- befree-2016 importedOn "2016-02-19" NP881743.RAj8l7-irHAwEbv7mYgexWhJXnCSbdyrNdf8WhTDFxTlY130_provenance.