Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_assertion wasGeneratedBy ECO_0000218 NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_assertion wasDerivedFrom ctd_human-2016 NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_assertion SIO_000772 19239083 NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_assertion evidence source_evidence_curated NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.
- NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_assertion description "[An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23588.RA4YbMbjqoPDiCzCXBA5-tqeVtDqlOVPCN8nTVPU2Zm20130_provenance.