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- source_evidence_literature type ECO_0000212 NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_assertion description "[ASXL1 haploinsufficiency is associated with a myelofibrosis phenotype in the context of other known and unknown lesions, and disruption of ASXL1 function may contribute to the disease pathogenesis of myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_assertion evidence source_evidence_literature NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_assertion SIO_000772 21712540 NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_assertion wasDerivedFrom befree-20150227 NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_assertion wasGeneratedBy ECO_0000203 NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978387.RAYf2K0TldO1UBkNV5I7gaTh7Fyicp6y3wkd97lypIGb0130_provenance.