Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion> ?p ?o ?g. }
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- NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion type Assertion NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_head.
- NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion description "[Achondroplasia (ACH), the most common form of human dwarfism, is caused by an activating autosomal dominant mutation in the fibroblast growth factor receptor-3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_provenance.
- NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion evidence source_evidence_literature NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_provenance.
- NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion SIO_000772 25650377 NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_provenance.
- NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion wasDerivedFrom befree-2016 NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_provenance.
- NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_assertion wasGeneratedBy ECO_0000203 NP1260896.RASnUUld8nXbje31ETrOP_HWZCHyUV8JYrQCDbx8XS2Nc130_provenance.