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- NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_assertion type Assertion NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_head.
- NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_assertion wasGeneratedBy ECO_0000203 NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_provenance.
- NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_assertion wasDerivedFrom befree-2016 NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_provenance.
- NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_assertion SIO_000772 21428921 NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_provenance.
- NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_assertion evidence source_evidence_literature NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_provenance.
- NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_assertion description "[Mutations in genes encoding either hamartin [TSC1 (tuberous sclerosis complex 1)] or tuberin (TSC2) result in a multisystem disorder characterized by the development of benign tumours and hamartomas in several organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881662.RA7rX1begG-Qy62uUXu1kX2y8-P34_e7H-Q6xdYPU0ds4130_provenance.