Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_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." NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_assertion evidence source_evidence_literature NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_assertion SIO_000772 23626758 NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_assertion wasDerivedFrom befree-20150227 NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_assertion wasGeneratedBy ECO_0000203 NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP943998.RAApFJFHAW7qSSjDX1Pi589Gg8Xh_QzPAOtNAqaMV3Ik0130_provenance.