Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_assertion type Assertion NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_head.
- NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_assertion description "[ASXL1 haploinsufficiency is associated with a myelofibrosis phenotype in the context of other known and unknown lesions, and disruption of ASXL1 function may contribute to the disease pathogenesis of myelofibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.
- NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_assertion evidence source_evidence_literature NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.
- NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_assertion SIO_000772 21712540 NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.
- NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_assertion wasDerivedFrom befree-2016 NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.
- NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_assertion wasGeneratedBy ECO_0000203 NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.