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- source_evidence_literature type ECO_0000212 NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_assertion description "[The absence of del(5q), trisomy 8 and 21, as well as the rarity of monosomy 7, contrasts with pooled published data and may reflect our exclusion of closely related disorders, in particular MDS with fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_assertion evidence source_evidence_literature NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_assertion SIO_000772 7819070 NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_assertion wasDerivedFrom befree-20150227 NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_assertion wasGeneratedBy ECO_0000203 NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914010.RAlWhsk5mOPPn3VNraJ3avyKHqGNOK5uEEMne5GB7bFBc130_provenance.