Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_assertion description "[TXNRD2 mutations may explain a fraction of human DCM disease burden.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_assertion evidence source_evidence_literature NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_assertion SIO_000772 21247928 NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_assertion wasDerivedFrom befree-20140225 NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_assertion wasGeneratedBy ECO_0000203 NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP445202.RAx3anxuKe-o2ABIiJaOmOu-5BtPf2Er_ImC7WLckivnc130_provenance.