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- source_evidence_literature type ECO_0000212 NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_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." NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion evidence source_evidence_literature NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion SIO_000772 14609921 NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion wasDerivedFrom befree-20150227 NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_assertion wasGeneratedBy ECO_0000203 NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877846.RAFMY6SRyVUPCsiRM13xdxzItw7P_UTU7rF8LosYii1PI130_provenance.