Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion description "[In conclusion, mutation of PRDM16 causes the cardiomyopathy in 1p36 deletion syndrome as well as a proportion of nonsyndromic LVNC and DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion evidence source_evidence_literature NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion SIO_000772 23768516 NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion wasDerivedFrom befree-20150227 NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_assertion wasGeneratedBy ECO_0000203 NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936424.RAvfJ3segLn4PFMaN_6G9zP_fOP6WmeyS5KpvfvP4kRFk130_provenance.