Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_assertion type Assertion NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_head.
- NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_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." NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_provenance.
- NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_assertion evidence source_evidence_literature NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_provenance.
- NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_assertion SIO_000772 11812941 NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_provenance.
- NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_assertion wasDerivedFrom befree-20150227 NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_provenance.
- NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_assertion wasGeneratedBy ECO_0000203 NP626742.RA5ZfBbdU6fDyEhxlDKdsOu1-_QXatiY7vhyUQOvJWgF0130_provenance.