Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_assertion type Assertion NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_head.
- NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_assertion description "[This study identified a novel disease-causing mutation p.R187C in MIP in a Chinese cataract family, expanding the mutation spectrum of MIP causing congenital cataract.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_provenance.
- NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_assertion evidence source_evidence_literature NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_provenance.
- NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_assertion SIO_000772 21245956 NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_provenance.
- NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_assertion wasDerivedFrom befree-20140225 NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_provenance.
- NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_assertion wasGeneratedBy ECO_0000203 NP909687.RAt-cicoYyO188Oh4EEY6fJvi5ZIq4d4NfBSO2cUhUM7s130_provenance.