Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_assertion> ?p ?o ?g. }
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- NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_assertion type Assertion NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_head.
- NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_assertion wasGeneratedBy ECO_0000203 NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_provenance.
- NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_assertion wasDerivedFrom befree-2016 NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_provenance.
- NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_assertion SIO_000772 22566713 NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_provenance.
- NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_assertion evidence source_evidence_literature NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_provenance.
- NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_assertion description "[Angelman syndrome due to a termination codon mutation of the UBE3A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980380.RABmYWkbS5SXPBcVs3SE3Gqzusqm2EATjCAIvTmfgN_Q0130_provenance.