Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion> ?p ?o ?g. }
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- NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion type Assertion NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_head.
- NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion wasGeneratedBy ECO_0000203 NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_provenance.
- NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion wasDerivedFrom befree-20150227 NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_provenance.
- NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion SIO_000772 20830319 NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_provenance.
- NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion evidence source_evidence_literature NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_provenance.
- NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_assertion description "[Phenylketonuria (PKU) is characterized by persistent hyperphenylalaninemia, due to mutations in the gene coding for phenylalanine hydroxylase (PAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606468.RAm5zuL4fckd63zjK-fM9STcHhdDatZVCh1Q5nYgy44VQ130_provenance.