Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_assertion> ?p ?o ?g. }
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- NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_assertion type Assertion NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_head.
- NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_assertion description "[Recently, a deletion mutation disrupting both TSC2 and PKD1 has been described in young children with tuberous sclerosis complex with severe renal cystic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_provenance.
- NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_assertion evidence source_evidence_literature NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_provenance.
- NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_assertion SIO_000772 11812941 NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_provenance.
- NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_assertion wasDerivedFrom befree-2016 NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_provenance.
- NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_assertion wasGeneratedBy ECO_0000203 NP343359.RA6UQ8XPejodruWg4tQzm_hcaK2S6PNxFnljrlPuxzM_M130_provenance.