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- NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_assertion type Assertion NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_head.
- NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_assertion wasGeneratedBy ECO_0000203 NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_provenance.
- NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_assertion wasDerivedFrom befree-20140225 NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_provenance.
- NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_assertion SIO_000772 20187763 NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_provenance.
- NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_assertion evidence source_evidence_literature NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_provenance.
- NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_assertion description "[Phenylalanine hydroxylase (PAH) deficiency is caused by mutations in the PAH gene resulting in a primary deficiency of the PAH enzyme activity, intolerance to the dietary intake of phenylalanine (Phe), and production of the phenylketonuria disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840888.RAbrH_CHxQONNFkmkq5oE2rRfnVSY5mQPEkfnPQe4E5TE130_provenance.