Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_assertion type Assertion NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_head.
- NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_assertion description "[Mouse models of XLAG, ISSX and other human ARX mutations demonstrate a direct genotype-phenotype correlation in ARX-related neurologic disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_provenance.
- NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_assertion evidence source_evidence_literature NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_provenance.
- NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_assertion SIO_000772 24236044 NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_provenance.
- NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_assertion wasDerivedFrom befree-2016 NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_provenance.
- NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_assertion wasGeneratedBy ECO_0000203 NP1128219.RAVoeC4Eosm1FG4eWtZ6GmwTjxt4CAjNcn15fot32ux8A130_provenance.