Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_assertion description "[It has recently been described that around half of RARS-T patients, along with a small subset of other MDS and mixed myelodysplastic/ myeloproliferative disorders, carry the JAK2 mutation, and that MPL mutations are found in single patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_assertion evidence source_evidence_literature NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_assertion SIO_000772 19074058 NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_assertion wasDerivedFrom befree-2016 NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_assertion wasGeneratedBy ECO_0000203 NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.
- befree-2016 importedOn "2016-02-19" NP708487.RACQJfmDBYRhs8pqIhvkDCVLgJuSPQAdhSJiKKNLsHeuY130_provenance.