Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP905685.RAcRcCuLf2GUqUoiSAby3V3RtADbulgS9SZuOvHuuvW9M130_provenance.