Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_assertion wasGeneratedBy ECO_0000203 NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_assertion wasDerivedFrom befree-20150227 NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_assertion SIO_000772 9731525 NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_assertion evidence source_evidence_literature NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.
- NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_assertion description "[Affected individuals in a multiplex pedigree with MRX (MRX30), previously mapped to Xq22, show a point mutation in the PAK3 (p21-activated kinase) gene, which encodes a serine-threonine kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374213.RAuXlQy2npPrx5lDrMPJIQe8Lr_o0mwdhfhLBfUSQDtfM130_provenance.