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- NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_assertion type Assertion NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_head.
- NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_assertion wasGeneratedBy ECO_0000203 NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_provenance.
- NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_assertion wasDerivedFrom befree-20140225 NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_provenance.
- NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_assertion SIO_000772 15007723 NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_provenance.
- NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_assertion evidence source_evidence_literature NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_provenance.
- NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_assertion description "[A TSC2-PKD1 contiguous gene syndrome caused by chromosomal microdeletions disrupting both the TSC2 and PKD1 genes has been identified in patients with TSC and early-onset severe ADPKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP712890.RATv1Abe0VQ8yoWxGx_AkU-H9iQKOZQePhrA9aC-ZngnI130_provenance.