Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_assertion wasGeneratedBy ECO_0000203 NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_assertion wasDerivedFrom befree-20140225 NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_assertion SIO_000772 17224687 NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_assertion evidence source_evidence_literature NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_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." NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP494138.RAe-mMWKgGqtnqRv93lEyTnHLSqa0IIWf4Z6Qm8JcHyQw130_provenance.