Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_assertion> ?p ?o ?g. }
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- NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_assertion type Assertion NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_head.
- NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_assertion wasGeneratedBy ECO_0000203 NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_provenance.
- NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_assertion wasDerivedFrom befree-20150227 NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_provenance.
- NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_assertion SIO_000772 23687350 NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_provenance.
- NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_assertion evidence source_evidence_literature NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_provenance.
- NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_assertion description "[Mutations in TSC1 or TSC2 cause the tuberous sclerosis complex (TSC), a disorder characterised by the development of hamartomas or benign tumours in various organs as well as the variable presence of epilepsy, intellectual disability (ID) and autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP759994.RAzWhFPtNiy0_49zLTiZ4zDylI-szjm6W441FYPxBl4_w130_provenance.