Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_assertion description "[To test the validity of this hypothesis, mutant human alpha 1-antitrypsin cDNA constructs coding for specific amino acid substitutions at residues 290 and 342 were generated and the corresponding mutant proteins were expressed in mouse hepatoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_assertion evidence source_evidence_literature NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_assertion SIO_000772 2563374 NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_assertion wasDerivedFrom befree-2016 NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_assertion wasGeneratedBy ECO_0000203 NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259396.RAeD_3n2RrDREMoMIWvQ6WFMxw8j4WnTRj_XT9sTXKvhU130_provenance.