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- NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_assertion type Assertion NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_head.
- NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_assertion wasGeneratedBy ECO_0000203 NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_provenance.
- NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_assertion wasDerivedFrom befree-2016 NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_provenance.
- NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_assertion SIO_000772 21428921 NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_provenance.
- NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_assertion evidence source_evidence_literature NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_provenance.
- NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_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." NP881659.RA4-nSGqSR_u5U6BS8MP5pki17kJtHY7l5e5BU_D8R6EA130_provenance.