Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_assertion description "[ASXL1 gene pathogenic mutations were also detected in three cases (two ET and one PMF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_assertion evidence source_evidence_literature NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_assertion SIO_000772 21904853 NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_assertion wasDerivedFrom befree-20150227 NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_assertion wasGeneratedBy ECO_0000203 NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978577.RA13LSApJbDFgwKtfMCmnqe39CWzoud5ImcUDF0JqEUcs130_provenance.