Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- befree-2016 importedOn "2016-02-19" NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_assertion wasGeneratedBy ECO_0000203 NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_assertion wasDerivedFrom befree-2016 NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_assertion SIO_000772 23160464 NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_assertion evidence source_evidence_literature NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.
- NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_assertion description "[Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029251.RADqjaHX2eF_W7_KYHkXS-q5Lo2INk7qOvnvwuBzrIR0o130_provenance.