Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP161993.RAAI2Ol58o0rLcwEvTprpppRlrajhrVoEKhUBfHuNHqUo130_provenance.