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- NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_assertion type Assertion NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_head.
- NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_assertion description "[Now, examination of the UGT1 gene structure in hyperbilirubinemic patients has revealed more than 100 different genetic defects in Crigler-Najjar syndromes and one genetic alternation that accounts for the majority of Gilbert's syndrome cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_provenance.
- NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_assertion evidence source_evidence_literature NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_provenance.
- NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_assertion SIO_000772 19845429 NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_provenance.
- NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_assertion wasDerivedFrom befree-2016 NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_provenance.
- NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_assertion wasGeneratedBy ECO_0000203 NP770714.RAFWI0V2qromnkviTeMjKD5qULAusvDBwcgE4J2fydTaY130_provenance.