Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_assertion description "[We have also documented that a high percentage of EGFR (67%), c-erbB2 (67%), p53 (75%) and cathepsin-D-positive DCIS (60%) were strongly positive for c-erbB3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_assertion evidence source_evidence_literature NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_assertion SIO_000772 9823984 NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_assertion wasDerivedFrom befree-2016 NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_assertion wasGeneratedBy ECO_0000203 NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1409261.RA3L7i6ufg9WqFLDevlRGgAOY7jcshssX9oVICMYAS0XI130_provenance.