Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_assertion description "[The folliculin-FNIP1 pathway deleted in human Birt-Hogg-Dub� syndrome is required for murine B-cell development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_assertion evidence source_evidence_literature NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_assertion SIO_000772 22709692 NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_assertion wasDerivedFrom befree-2016 NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_assertion wasGeneratedBy ECO_0000203 NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.
- befree-2016 importedOn "2016-02-19" NP990992.RAxGQ4D4_DLYvwZG6oUjs4NFKNVRK4lXkojttC5CYenbU130_provenance.