Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP608612.RARE4giOI1arylwcIT5NMwXokz11VcZH_mPqUM48RnDpI130_provenance.