Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_assertion description "[Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_assertion evidence source_evidence_curated NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_assertion SIO_000772 12704386 NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_assertion wasDerivedFrom uniprot-20130724 NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_assertion wasGeneratedBy ECO_0000218 NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP658.RAGOqIc3PWspm0Y3GJYaHe6Ah5jGhNXy-VCDI11q4_5Qw130_provenance.