Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_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." NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_assertion evidence source_evidence_literature NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_assertion SIO_000772 23341106 NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_assertion wasDerivedFrom befree-20150227 NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_assertion wasGeneratedBy ECO_0000203 NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP541766.RAiud2Bb0WJB3TbZLltCiTvyWI1c3EZvjOh99s9U8STZY130_provenance.