Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_assertion description "[May-Hegglin anomaly (MHA), Sebastian (SBS), Fechtner (FTNS) and Epstein (EPS) syndromes are rare autosomal dominant disorders with giant platelets and thrombocytopenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_assertion evidence source_evidence_literature NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_assertion SIO_000772 18925516 NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_assertion wasDerivedFrom befree-20140225 NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_assertion wasGeneratedBy ECO_0000203 NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.
- befree-20140225 importedOn "2014-02-25" NP343490.RAJVP9I77-pjpf0a5d5hBQEgWm4e-knGSjzH7ic350cww130_provenance.