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- source_evidence_literature type ECO_0000212 NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_assertion description "[SDHB protein expression was absent in all 102 phaeochromocytomas and paragangliomas with an SDHB, SDHC, or SDHD mutation, but was present in all 65 paraganglionic tumours related to multiple endocrine neoplasia type 2, von Hippel-Lindau disease, and neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_assertion evidence source_evidence_literature NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_assertion SIO_000772 19576851 NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_assertion wasDerivedFrom befree-2016 NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_assertion wasGeneratedBy ECO_0000203 NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.
- befree-2016 importedOn "2016-02-19" NP749158.RAz5jQ_zFYFCOlVPKWhRW1oPWDi3ynlxw4eWCMlha1HsM130_provenance.