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- NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_assertion type Assertion NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_head.
- NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_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." NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_provenance.
- NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_assertion evidence source_evidence_literature NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_provenance.
- NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_assertion SIO_000772 19845429 NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_provenance.
- NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_assertion wasDerivedFrom befree-20150227 NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_provenance.
- NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_assertion wasGeneratedBy ECO_0000203 NP912465.RAFRmgCrAvmPI5eMgzkXcPBJEhr-AW5F342ayN4i5fo_I130_provenance.