Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_assertion description "[Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at least three genetic subtypes (USH2A, USH2B, and USH2C) and is classified phenotypically as congenital hearing loss and progressive retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_assertion evidence source_evidence_literature NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_assertion SIO_000772 14740321 NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_assertion wasDerivedFrom befree-20140225 NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_assertion wasGeneratedBy ECO_0000203 NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722465.RAkjd6wYQR2tSGbj3OaIBJEDR1GfWz5xj1p1F1ENLQ8f0130_provenance.