Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_assertion> ?p ?o ?g. }
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- NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_assertion type Assertion NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_head.
- NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_assertion wasGeneratedBy ECO_0000203 NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_provenance.
- NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_assertion wasDerivedFrom gad-20150221 NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_provenance.
- NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_assertion SIO_000772 11517203 NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_provenance.
- NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_assertion evidence source_evidence_literature NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_provenance.
- NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_assertion description "[ Most patients with symptomatic MCAD deficiency could be detected by newborn screening. Infants actually detected had a lower frequency of A985G alleles than clinically diagnosed cases and may have a lower risk of becoming symptomatic.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76498.RAickqs0CtGDTrBmiKAt_rE6c6xHQnE8fRv9IfW1z8ef0130_provenance.