Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_assertion description "[Some patients with primary hereditary erythrocytosis exhibit a mutation in the erythropoietin receptor (EPOR) which is associated with low serum erythropoietin (EPO) levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_assertion evidence source_evidence_literature NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_assertion SIO_000772 25189721 NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_assertion wasDerivedFrom befree-2016 NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_assertion wasGeneratedBy ECO_0000203 NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216999.RAdF5SrUqWHWXywnmL62RjCa-QsNc2R4Ji-9gj2Zfn-NA130_provenance.