Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_assertion> ?p ?o ?g. }
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- NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_assertion type Assertion NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_head.
- NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_assertion description "[Most probably the lack of mutated SLC22A4 substrate explains the absence of RUNX1 association with RA observed in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_provenance.
- NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_assertion evidence source_evidence_literature NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_provenance.
- NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_assertion SIO_000772 16652416 NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_provenance.
- NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_assertion wasDerivedFrom befree-20150227 NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_provenance.
- NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_assertion wasGeneratedBy ECO_0000203 NP701803.RAAyuaST9X72N-LQGwhO6ZH7ChR-P6C6ss6vUMHTFcyrI130_provenance.