Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_assertion wasGeneratedBy ECO_0000203 NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_assertion wasDerivedFrom befree-20150227 NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_assertion SIO_000772 22890969 NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_assertion evidence source_evidence_literature NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.
- NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_assertion description "[TP53 mutations and 1p19q codeletion are the main molecular abnormalities recorded, respectively, in astrocytomas and oligodendrogliomas and in mixed gliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753700.RAaZPRIdbdbCXKtEykXtf1Z0-0TzUsrNFn_s3sSxVN3zg130_provenance.