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- source_evidence_literature type ECO_0000212 NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_assertion description "[Altogether, RUNX1 dosage could explain the differential phenotype according to RUNX1 mutations, with a haploinsufficiency leading to thrombocytopenia alone in a majority of cases whereas a more complete gene deletion predisposes to leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_assertion evidence source_evidence_literature NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_assertion SIO_000772 25490895 NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_assertion wasDerivedFrom befree-2016 NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_assertion wasGeneratedBy ECO_0000203 NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246487.RA8PCYVbyANwznnp0HTSvV2grbDBWPJ01200sj5U3EHOY130_provenance.