Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_assertion description "[CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_assertion evidence source_evidence_curated NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_assertion SIO_000772 18445044 NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_assertion wasDerivedFrom uniprot-2016 NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_assertion wasGeneratedBy ECO_0000218 NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP5364.RAlmZK9Ut6ID9XkI54LFvn2jzRHCKK_vGYtllIp61gcWg130_provenance.