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- NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_assertion type Assertion NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_head.
- NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_assertion description "[The HFE mutations associated with Hereditary Haemochromatosis are not more common in Irish CD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_provenance.
- NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_assertion evidence source_evidence_literature NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_provenance.
- NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_assertion SIO_000772 16615226 NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_provenance.
- NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_assertion wasDerivedFrom gad-20150221 NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_provenance.
- NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_assertion wasGeneratedBy ECO_0000203 NP100050.RAQLRuW20GMdwPVtFEkW0NTVz22EcYv2Gu-3COKnQQ0L0130_provenance.