Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_assertion description "[The 208delG mutation in the FSCN2 gene produces not only autosomal dominant retinitis pigmentosa but also ADMD in the Japanese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_assertion evidence source_evidence_literature NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_assertion SIO_000772 14609921 NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_assertion wasDerivedFrom befree-20140225 NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_assertion wasGeneratedBy ECO_0000203 NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP808767.RA_bMt-ctrTeCh3n6TjRQJM7Rku4CH_ogBddoQC_af49w130_provenance.