Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_assertion description "[No patients had mutations of Park2 or MAPT but there was genetic association for the polymorphism Val380Leu in sporadic and familial PSP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_assertion evidence source_evidence_literature NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_assertion SIO_000772 18022644 NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_assertion wasDerivedFrom gad-20150221 NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_assertion wasGeneratedBy ECO_0000203 NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP115330.RAGVgCtLK8Yca3FDbDwXl2qQLn-K6LeKmsBCrx0X-p_aU130_provenance.