Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_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." NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_assertion evidence source_evidence_literature NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_assertion SIO_000772 14592816 NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_assertion wasDerivedFrom lhgdn-20090331 NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_assertion wasGeneratedBy ECO_0000203 NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP202000.RAuGxEvmeHFH_pZtBpwv7QhQbOXDPXBNESZDSRcZF8ca0130_provenance.