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- source_evidence_literature type ECO_0000212 NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_assertion description "[After reclassification, MYD88 L265P was detected in 13/86 (15%) SMZL and in 19/24 LPL (79%) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_assertion evidence source_evidence_literature NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_assertion SIO_000772 25723115 NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_assertion wasDerivedFrom befree-2016 NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_assertion wasGeneratedBy ECO_0000203 NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266741.RAGaKMjTPpAjougua5A8k_Ego_w_LkivRiG5mifvMwhzE130_provenance.