Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_assertion description "[We detected methylation differences in pathways related to heart disease, but also in genes with yet unknown function in DCM or heart failure, namely Lymphocyte antigen 75 (LY75), Tyrosine kinase-type cell surface receptor HER3 (ERBB3), Homeobox B13 (HOXB13) and Adenosine receptor A2A (ADORA2A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_assertion evidence source_evidence_literature NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_assertion SIO_000772 23341106 NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_assertion wasDerivedFrom befree-20140225 NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_assertion wasGeneratedBy ECO_0000203 NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP923683.RA4WH4dWH8eiXUfjDv--3-H3YwHZM5fan8wu2jeZLG9pc130_provenance.