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- source_evidence_literature type ECO_0000212 NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- befree-2016 importedOn "2016-02-19" NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_assertion wasGeneratedBy ECO_0000203 NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_assertion wasDerivedFrom befree-2016 NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_assertion SIO_000772 10939445 NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_assertion evidence source_evidence_literature NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.
- NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_assertion description "[Using fluorescently labeled allele-specific primers, the S65C (193A-->T) substitution associated with hereditary haemochromatosis in the HFE gene is genotyped.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291798.RABtlMWhCz2q4eI4CJS7S1ae_ig6pSsE_8i4VVxD-KuaE130_provenance.