Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_assertion> ?p ?o ?g. }
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- NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_assertion type Assertion NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_head.
- NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_assertion description "[A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_provenance.
- NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_assertion evidence source_evidence_literature NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_provenance.
- NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_assertion SIO_000772 10053006 NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_provenance.
- NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_assertion wasDerivedFrom befree-20140225 NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_provenance.
- NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_assertion wasGeneratedBy ECO_0000203 NP534019.RA1x1J_-K10nFKRxIENV7MhAyXIsaITrWR7JFc_TDR3WA130_provenance.