Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_assertion description "[Rare variants in these 5 genes likely or possibly caused 10.6% of DCM in this cohort. When combined with our prior resequencing reports, approximately 27% of DCM probands had possible or likely disease-causing variants identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_assertion evidence source_evidence_literature NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_assertion SIO_000772 20215591 NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_assertion wasDerivedFrom gad-20150221 NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_assertion wasGeneratedBy ECO_0000203 NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP121322.RAA_0JLLoShrh6ic5GRoXnmQyl6V0bxt4csCH-tM2NXZc130_provenance.