Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_assertion description "[Two of the six patients harbouring STX11 gene defects developed myelodysplastic syndrome (MDS) or acute myelogenous leukaemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_assertion evidence source_evidence_literature NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_assertion SIO_000772 16582076 NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_assertion wasDerivedFrom befree-2016 NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_assertion wasGeneratedBy ECO_0000203 NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.
- befree-2016 importedOn "2016-02-19" NP543052.RA9kD6OpK-4iskhSYHz0-6b0D4jSuYNS7ooTNry7wmDdU130_provenance.