Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_assertion> ?p ?o ?g. }
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- NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_assertion type Assertion NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_head.
- NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_assertion description "[Tuberous Sclerosis Complex (TSC) is a genetic disorder that occurs through the loss of heterozygosity of either TSC1 or TSC2, which encode Hamartin or Tuberin, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_provenance.
- NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_assertion evidence source_evidence_literature NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_provenance.
- NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_assertion SIO_000772 12906785 NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_provenance.
- NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_assertion wasDerivedFrom befree-2016 NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_provenance.
- NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_assertion wasGeneratedBy ECO_0000203 NP404690.RAVsYDNxDsn3Nnw4sjdbWEQu3SB3TVMhDm_OMfFaq81BY130_provenance.