Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_assertion description "[Although NF-E2 levels correlate with JAK2(V671F) allele burden in some PV cohorts, the molecular mechanism causing aberrant NF-E2 expression has not been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_assertion evidence source_evidence_literature NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_assertion SIO_000772 20339092 NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_assertion wasDerivedFrom befree-20140225 NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_assertion wasGeneratedBy ECO_0000203 NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP776830.RA1rvWZGVlkhS109oNu056UluqStTlg7I_U4W1y5_PnVk130_provenance.