Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_assertion type Assertion NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_head.
- NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_assertion description "[In contrast, when the inheritance is complex, the epileptic phenotype is determined by several minor genetic defects that are much more difficult to discover.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_provenance.
- NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_assertion evidence source_evidence_literature NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_provenance.
- NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_assertion SIO_000772 18754913 NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_provenance.
- NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_assertion wasDerivedFrom befree-2016 NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_provenance.
- NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_assertion wasGeneratedBy ECO_0000203 NP690257.RAD7SpTQUcnoI3XIhwWP_rx6aFrouN2eaKIjyhByEBtuk130_provenance.