Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_assertion description "[Haplotype analysis of the Brown syndrome phenotype was consistent with recessive inheritance at the DURS1 locus and dominant inheritance with reduced penetrance at the DURS1, DURS2, and FEOM1 loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_assertion evidence source_evidence_literature NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_assertion SIO_000772 12324876 NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_assertion wasDerivedFrom befree-20140225 NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_assertion wasGeneratedBy ECO_0000203 NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP358239.RADV2htava06NY1cmRtCChyOuYqsnOfw8A9Dtqgr2AOwI130_provenance.