Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_assertion description "[It was recently discovered that many of the underlying mutations responsible for the familial form of WPW syndrome are located in the gene encoding for the regulatory gamma(2)-subunit (PRKAG2) of the AMP-activated protein kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_assertion evidence source_evidence_literature NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_assertion SIO_000772 16686673 NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_assertion wasDerivedFrom befree-20150227 NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_assertion wasGeneratedBy ECO_0000203 NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP247423.RAG8VYKwFD3pQDybNtME7IiFLkV_Cd6OiT0h3YsvSydyA130_provenance.