Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_assertion description "[Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_assertion evidence source_evidence_curated NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_assertion SIO_000772 20215591 NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_assertion wasDerivedFrom uniprot-2016 NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_assertion wasGeneratedBy ECO_0000218 NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6142.RAjxfXeX9AoHfukaE3BX9WXcqz36ILwFSFoLfT530kRu0130_provenance.