Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_assertion description "[series of novel point mutations in ATRX detected in archival DNA samples from marrow and/or blood of patients with myelodysplastic syndrome associated with alpha-thalassemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_assertion evidence source_evidence_literature NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_assertion SIO_000772 14592816 NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_assertion wasDerivedFrom lhgdn-20090331 NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_assertion wasGeneratedBy ECO_0000203 NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP125476.RATsaU3nFm8W1jFvqdfCQo8NFZ589oNYjW8ruNeCBSVic130_provenance.