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- NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_assertion type Assertion NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_head.
- NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_assertion wasGeneratedBy ECO_0000203 NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.
- NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_assertion wasDerivedFrom befree-20140225 NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.
- NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_assertion SIO_000772 21636066 NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.
- NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_assertion evidence source_evidence_literature NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.
- NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_assertion description "[Thus, FYCO1 is involved in lens development and transparency in humans, and mutations in this gene are one of the most common causes of arCC in the Pakistani population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.