Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_assertion description "[Both DCM-associated mutations result in amino acid substitutions of highly conserved residues in helices contributing to the flavin-adenine dinucleotide (FAD)-binding domain of TXNRD2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_assertion evidence source_evidence_literature NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_assertion SIO_000772 21247928 NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_assertion wasDerivedFrom befree-20140225 NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_assertion wasGeneratedBy ECO_0000203 NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP545554.RA0e0bE6kapUP2eqZc4v3aQu7nvVEvlNbkN0Zr8rNfQPw130_provenance.