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- source_evidence_literature type ECO_0000212 NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_assertion description "[Mutations of JAK2(V617F) or MPL(W515K/L) were absent in pediatric patients with PMF according to previous studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_assertion evidence source_evidence_literature NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_assertion SIO_000772 25176567 NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_assertion wasDerivedFrom befree-2016 NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_assertion wasGeneratedBy ECO_0000203 NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215850.RADM0a8MqLzawhWbsnBce_lPIMexNoicExW2P-gfcbUPA130_provenance.