Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_assertion> ?p ?o ?g. }
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- NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_assertion type Assertion NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_head.
- NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_assertion wasGeneratedBy ECO_0000203 NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_provenance.
- NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_assertion wasDerivedFrom befree-20140225 NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_provenance.
- NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_assertion SIO_000772 23428682 NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_provenance.
- NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_assertion evidence source_evidence_literature NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_provenance.
- NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_assertion description "[A patient with a mutation that led to a partially functional protein had a less severe growth phenotype and no deafness, similarly to two siblings with a heterozygous IGF1 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660722.RA4UBVXd31P97dUAfI14Naon-N785jZkImy2IYBuGOxiY130_provenance.