Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_assertion description "[Patients with a deletion of 4 consecutive amino acids in the gene encoding for the alpha(2C)-adrenergic receptor (alpha(2C)Del322-325) have an increased prevalence of clinical heart failure, worse clinical status, and a lower left ventricular ejection fraction compared with patients without this deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_assertion evidence source_evidence_literature NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_assertion SIO_000772 14668769 NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_assertion wasDerivedFrom befree-20150227 NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_assertion wasGeneratedBy ECO_0000203 NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP226604.RA-4OgMiCQ8rxlicjygenTwyHDDc_BWbVEiVDE7v_EVf0130_provenance.