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- source_evidence_literature type ECO_0000212 NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_assertion description "[We identified chromosomal deletions within the WASP gene in two patients with Wiskott-Aldrich syndrome; a missense mutation in a patient with X-linked thrombocytopenia; and mutations in the RUNX1 gene of five patients with familial platelet disorder with propensity to acute myelogenous leukemia, and in the ANKRD26 gene of four patients with autosomal dominant thrombocytopenia-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_assertion evidence source_evidence_literature NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_assertion SIO_000772 26175287 NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_assertion wasDerivedFrom befree-2016 NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_assertion wasGeneratedBy ECO_0000203 NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1290142.RAopO0axpxFy8HkinWkO4tVYhtHOBgaEGYtmNNLb-Y2OY130_provenance.