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- source_evidence_literature type ECO_0000212 NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_assertion description "[Routine germline MEN1 mutation testing of all cases of ' classical ' MEN1, familial hyperparathyroidism, and sporadic hyperparathyroidism with one other MEN1 related condition is justified by national testing services.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_assertion evidence source_evidence_literature NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_assertion SIO_000772 15635078 NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_assertion wasDerivedFrom lhgdn-20090331 NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_assertion wasGeneratedBy ECO_0000203 NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193968.RA5Pe5YSs8x00AlblcnCCTZdYYp0K_EBSLWkhVBBS_jyM130_provenance.