Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_assertion description "[Familial expansile osteolysis, early-onset familial PDB and expansile skeletal hyperphosphatasia are related disorders caused by mutations affecting the TNFRSF11A gene, which encodes the receptor activator of NFkappaB (RANK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_assertion evidence source_evidence_literature NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_assertion SIO_000772 18328984 NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_assertion wasDerivedFrom befree-20140225 NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_assertion wasGeneratedBy ECO_0000203 NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP276913.RAcAQYXOMCa6Z8XUky02006Ll20P7CCEePQVy31XWhlyg130_provenance.