Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- befree-2016 importedOn "2016-02-19" NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_assertion wasGeneratedBy ECO_0000203 NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_assertion wasDerivedFrom befree-2016 NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_assertion SIO_000772 17224687 NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_assertion evidence source_evidence_literature NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.
- NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_assertion description "[Large overlapping cDNA fragments from KCNQ1 and KCNH2 (Long QT Syndrome), MYBPC3 (hypertrophic and dilated cardiomyopathy), or FBN1 (Marfan Syndrome) were amplified from RNA and directly sequenced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589015.RAqrAw1n0v1V1IGWPa7Gvb2_wU5DHHguOpgTga6hBKURo130_provenance.