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- source_evidence_literature type ECO_0000212 NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_assertion description "[Using serial banked samples and quantitative ASXL1 mutant allele burden assays, we observed the acquisition and accumulation of ASXL1 mutations over time in two patients with post-essential thrombocytosis myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_assertion evidence source_evidence_literature NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_assertion SIO_000772 21712540 NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_assertion wasDerivedFrom befree-2016 NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_assertion wasGeneratedBy ECO_0000203 NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.
- befree-2016 importedOn "2016-02-19" NP905687.RAWSxN-YtDVd_d4HKPiiBRmN_3udWwh9mDm8t1FT8eDO0130_provenance.