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- NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_assertion type Assertion NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_head.
- NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_assertion wasGeneratedBy ECO_0000203 NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_provenance.
- NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_assertion wasDerivedFrom befree-20140225 NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_provenance.
- NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_assertion SIO_000772 10698592 NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_provenance.
- NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_assertion evidence source_evidence_literature NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_provenance.
- NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_assertion description "[The identification of the gene(s) causing FGD without mutations in the MC2-R and causing the triple A syndrome may reveal novel aspects in cell signalling and neuroendocrinology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548819.RAiiGjEXCTv6W7PLnbadKc2Z9OIG513YbKfJaoAbGM14I130_provenance.