Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- befree-2016 importedOn "2016-02-19" NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_assertion wasGeneratedBy ECO_0000203 NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_assertion wasDerivedFrom befree-2016 NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_assertion SIO_000772 20578134 NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_assertion evidence source_evidence_literature NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.
- NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_assertion description "[RUNX1 gene is responsible for an autosomal dominant platelet disorder with predisposition to acute myelogenous leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821398.RA88lFkPMoYW47Ba0q7pzvmp-bmQhSpfMUdkXBO-gs-lw130_provenance.