Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_assertion> ?p ?o ?g. }
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- NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_assertion type Assertion NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_head.
- NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_assertion wasGeneratedBy ECO_0000203 NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_provenance.
- NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_assertion wasDerivedFrom befree-20140225 NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_provenance.
- NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_assertion SIO_000772 12768443 NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_provenance.
- NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_assertion evidence source_evidence_literature NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_provenance.
- NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_assertion description "[Wiedemann-Rautenstrauch syndrome (WRS; MIM 264090) is another extremely rare disease that is characterized by progeroid features from birth with multiple somatic anomalies and paucity of subcutaneous fat.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP231542.RAZkBhADaCrTIBdjnTFEZhL1PxFDV2nWn1yT1bDMgABGA130_provenance.