Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_assertion type Assertion NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_head.
- NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_assertion description "[In 1994, the field of bone biology was significantly advanced by the discovery that activating mutations in the fibroblast growth factor receptor 3 (FGFR3) receptor tyrosine kinase (TK) account for the common genetic form of dwarfism in humans, achondroplasia (ACH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_provenance.
- NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_assertion evidence source_evidence_literature NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_provenance.
- NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_assertion SIO_000772 22045636 NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_provenance.
- NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_assertion wasDerivedFrom befree-20140225 NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_provenance.
- NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_assertion wasGeneratedBy ECO_0000203 NP349458.RAmZl__h4UZQl0Gzv6ptNeW3s3nhSzUqesYOwJ2UBAzOU130_provenance.