Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_assertion description "[Individuals who came from two families and met the diagnostic criteria for WMS were each found to have a different homozygous missense mutation in ADAMTS10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_assertion evidence source_evidence_literature NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_assertion SIO_000772 19836009 NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_assertion wasDerivedFrom befree-2016 NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_assertion wasGeneratedBy ECO_0000203 NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.
- befree-2016 importedOn "2016-02-19" NP769787.RAbm5ZZdlYmUC9Kq09IudMBK0WthJtu5nwe68QBXUWwzs130_provenance.