Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_assertion description "[IL-12R?1 deficiency, also known as immunodeficiency 30 (IMD30, OMIM 614891), is a rare immunodeficiency syndrome caused by biallelic mutations in IL12RB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_assertion evidence source_evidence_literature NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_assertion SIO_000772 25467645 NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_assertion wasDerivedFrom befree-2016 NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_assertion wasGeneratedBy ECO_0000203 NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244182.RAKjhDWiMzC8bHs8CxCmK5fJQdaPCg_6PmHcruJDSnLZc130_provenance.