Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion type Assertion NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_head.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion description "[This study reaffirms the view that large MECP2 deletions are an important cause of both classical and atypical Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion evidence source_evidence_literature NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion SIO_000772 17712354 NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion wasDerivedFrom lhgdn-20090331 NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.
- NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_assertion wasGeneratedBy ECO_0000203 NP228447.RAEHKXBfKF_turi8ztOSHaEHq4FrIcT_VPYTSxt7zKBKI130_provenance.