Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_assertion description "[We have studied the mutational status of TET2 (complete coding region), ASXL1 (exon12), IDH1 (R132), IDH2 (R140 and R172), and c-CBL (exons 8 and 9) in 62 MPN patients (52 essential thrombocythemia (ET), five polycythemia vera (PV), and five primary myelofibrosis (PMF)) negative for both JAK2 (V617F and exon 12) and MPL (exon 10) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_assertion evidence source_evidence_literature NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_assertion SIO_000772 21904853 NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_assertion wasDerivedFrom befree-2016 NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_assertion wasGeneratedBy ECO_0000203 NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.
- befree-2016 importedOn "2016-02-19" NP922471.RA1MmXc60lS9ZrUXdCbKAkRKokrWNQPSOk9zWo2RSciVo130_provenance.