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- source_evidence_literature type ECO_0000212 NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_assertion description "[The remaining cases usually lack the JAK2(V617F)mutation, have a platelet count less than 600 � 10(3)/?L (600 � 10(9)/L), and may represent an MDS or MPN with thrombocytosis of unknown mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_assertion evidence source_evidence_literature NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_assertion SIO_000772 21350094 NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_assertion wasDerivedFrom befree-2016 NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_assertion wasGeneratedBy ECO_0000203 NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.
- befree-2016 importedOn "2016-02-19" NP875057.RADjaAeyR9ZKCV8x3EYY1bdHNIHmhRvSGZj-uZNFKpf2I130_provenance.