Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_assertion description "[Clonality investigation including mutational status of MPL, TET2, and ASXL1 genes and human androgen receptor (HUMARA) assay was performed in 73 JAK2V617F-negative cases out of 186 subjects consecutively diagnosed with ET in a single institution, at diagnosis or during follow-up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_assertion evidence source_evidence_literature NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_assertion SIO_000772 22706669 NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_assertion wasDerivedFrom befree-2016 NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_assertion wasGeneratedBy ECO_0000203 NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.
- befree-2016 importedOn "2016-02-19" NP990841.RA6HdZUlWvNPOcArrx1dmFToeG_Oiqx6VM9UWCll5IpuI130_provenance.