Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_assertion description "[Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_assertion evidence source_evidence_curated NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_assertion SIO_000772 11487566 NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_assertion wasDerivedFrom uniprot-2016 NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_assertion wasGeneratedBy ECO_0000218 NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1565.RAp7Ktz_hNAg68Bj-R33fcMQiNQpNc-8pfolfhQOMMsaM130_provenance.