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- source_evidence_literature type ECO_0000212 NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_assertion description "[Familial isolated primary hyperparathyroidism is a distinct genetic variant of the MEN1 syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_assertion evidence source_evidence_literature NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_assertion SIO_000772 18084346 NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_assertion wasDerivedFrom lhgdn-20090331 NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_assertion wasGeneratedBy ECO_0000203 NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193981.RA-wjCTF0fGAQ0gcUgny25DY_LSefFpn0S7n5Euiycy7g130_provenance.