Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_assertion description "[In addition to JAK2 mutations, several genetic abnormalities, including TET2 and polycomb group genes involving epigenetic regulation have been reported in patients with MPN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_assertion evidence source_evidence_literature NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_assertion SIO_000772 23237864 NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_assertion wasDerivedFrom befree-20140225 NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_assertion wasGeneratedBy ECO_0000203 NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615659.RAeL-8whW_ro5PuB6soGjr7xCpPBEGZhrDrNqIQv2gWCo130_provenance.