Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_assertion description "[Inherited or sporadic heterozygous mutations in the transcription factor GATA2 lead to a clinical syndrome characterized by non-tuberculous mycobacterial and other opportunistic infections, a severe deficiency in monocytes, B cells and natural killer cells, and progression from a hypocellular myelodysplastic syndrome to myeloid leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_assertion evidence source_evidence_literature NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_assertion SIO_000772 24077845 NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_assertion wasDerivedFrom befree-2016 NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_assertion wasGeneratedBy ECO_0000203 NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1114757.RAD01kOSNetNVrid0GPZMtqFnV9A6EtVC2xfnFNpfE2fY130_provenance.