Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_assertion> ?p ?o ?g. }
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- NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_assertion type Assertion NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_head.
- NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_assertion description "[RSK4 is completely deleted in eight patients with the contiguous gene syndrome including MRX, partially deleted in a patient with DFN3 and present in patients with an Xq21 deletion and normal intellectual abilities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_provenance.
- NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_assertion evidence source_evidence_literature NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_provenance.
- NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_assertion SIO_000772 10644430 NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_provenance.
- NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_assertion wasDerivedFrom befree-20140225 NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_provenance.
- NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_assertion wasGeneratedBy ECO_0000203 NP250536.RAEU9Nn_zA2JR0K1R8aA_HcRiDArlPVDVQX1Xux0vnjqI130_provenance.