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- source_evidence_literature type ECO_0000212 NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_assertion description "[Patients with NF1 and MEN 2 could be discriminated from those with VHL, SDHB, and SDHD gene mutations in 99% of cases by the combination of normetanephrine and metanephrine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_assertion evidence source_evidence_literature NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_assertion SIO_000772 21262951 NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_assertion wasDerivedFrom befree-20150227 NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_assertion wasGeneratedBy ECO_0000203 NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP689101.RAa2TpNI4Ek46k2K31xAZbWCrGJsFWUN-V85_15J_EfoU130_provenance.