Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_assertion description "[Mutations in ANKRD11 have recently been reported to cause KBG syndrome, an autosomal dominant condition characterized by intellectual disability (ID), behavioral problems, and macrodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_assertion evidence source_evidence_literature NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_assertion SIO_000772 25413698 NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_assertion wasDerivedFrom befree-2016 NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_assertion wasGeneratedBy ECO_0000203 NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238999.RABigq3Q_ldJIr7zdwj0c_h5h_1eIa7NH4ow241AZCF60130_provenance.