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- NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_assertion type Assertion NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_head.
- NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_assertion description "[31 different germline FH mutations in 56 families with Hereditary leiomyomatosis and renal cell cancer (HLRCC) (20 missense, eight frameshifts, two nonsense, and one splice site) was indentified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_provenance.
- NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_assertion evidence source_evidence_literature NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_provenance.
- NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_assertion SIO_000772 15937070 NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_provenance.
- NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_assertion wasDerivedFrom lhgdn-20090331 NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_provenance.
- NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_assertion wasGeneratedBy ECO_0000203 NP211242.RA45NldH3Rnm1l02besd9iekpYOCEzDeg_wZ5aNvehhsg130_provenance.