Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_assertion type Assertion NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_head.
- NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_assertion description "[The molecular defects associated with Angelman syndrome (AS) and 15q duplication autism are directly correlated to expression levels of the E3 ubiquitin ligase protein UBE3A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.
- NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_assertion evidence source_evidence_literature NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.
- NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_assertion SIO_000772 23626758 NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.
- NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_assertion wasDerivedFrom befree-20150227 NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.
- NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_assertion wasGeneratedBy ECO_0000203 NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.