Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_assertion description "[Three frameshift mutations of ASXL1 leading to a truncated protein were found in three patients (4%) with late onset JMML displaying also RAS activating mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_assertion evidence source_evidence_literature NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_assertion SIO_000772 20955399 NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_assertion wasDerivedFrom befree-2016 NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_assertion wasGeneratedBy ECO_0000203 NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.
- befree-2016 importedOn "2016-02-19" NP846456.RAiF1sEjYS1YTvL8yJ1fKoSbVhxeRSrB6_mLyxabGC90E130_provenance.