Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_assertion description "[Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_assertion evidence source_evidence_literature NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_assertion SIO_000772 8402893 NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_assertion wasDerivedFrom befree-2016 NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_assertion wasGeneratedBy ECO_0000203 NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1340965.RAAtLs6pwg3ysLySebm731QSVcO1hnGLdOENIA2AdRK8U130_provenance.