Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_assertion description "[Absence of mutations in the granulocyte colony-stimulating factor (G-CSF) receptor gene in patients with myelodysplastic syndrome/acute myeloblastic leukaemia occurring after treatment of aplastic anaemia with G-CSF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_assertion evidence source_evidence_literature NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_assertion SIO_000772 11122117 NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_assertion wasDerivedFrom befree-20140225 NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_assertion wasGeneratedBy ECO_0000203 NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP836016.RA9_OKU4-OhqdAkeNRCccfiUhs3GwP5LY3wTojC3k-bEo130_provenance.