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- NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_assertion type Assertion NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_head.
- NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_assertion wasGeneratedBy ECO_0000203 NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_provenance.
- NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_assertion wasDerivedFrom befree-20140225 NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_provenance.
- NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_assertion SIO_000772 14604959 NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_provenance.
- NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_assertion evidence source_evidence_literature NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_provenance.
- NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_assertion description "[The first congenital defect of hypoxia-sensing homozygosity for VHL 598C>T mutation was recently identified in Chuvash polycythemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_provenance.