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- NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_assertion type Assertion NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_head.
- NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_assertion description "[Acanthosis nigricans is a feature of several syndromes caused by activating mutations of the fibroblast growth factor receptor 3 gene (FGFR3), including Crouzon syndrome with acanthosis nigricans, thanatophoric dysplasia, and severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_provenance.
- NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_assertion evidence source_evidence_literature NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_provenance.
- NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_assertion SIO_000772 17875876 NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_provenance.
- NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_assertion wasDerivedFrom befree-2016 NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_provenance.
- NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_assertion wasGeneratedBy ECO_0000203 NP630576.RAM_HSM5oJrfkKb7uvxVtWJoon-rGlvFeLcrKWY2CU6hc130_provenance.