Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion description "[The JAK2 V617F point mutation is very rare in hypereosinophilic syndrome and/or chronic eosinophilic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion evidence source_evidence_literature NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion SIO_000772 18024388 NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion wasDerivedFrom befree-2016 NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_assertion wasGeneratedBy ECO_0000203 NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.
- befree-2016 importedOn "2016-02-19" NP641073.RAiYTehnM7jllJJ20Cs_wQms6NoUkohpAzxap7l4r0tDs130_provenance.