Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_assertion> ?p ?o ?g. }
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- NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_assertion type Assertion NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_head.
- NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_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." NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_provenance.
- NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_assertion evidence source_evidence_literature NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_provenance.
- NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_assertion SIO_000772 17875876 NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_provenance.
- NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_assertion wasDerivedFrom befree-20150227 NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_provenance.
- NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_assertion wasGeneratedBy ECO_0000203 NP401285.RAWqbQtI4lF6TKQyDScKr2Qb2suMfmiPqVzoJvBrvcYRo130_provenance.