Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_assertion wasGeneratedBy ECO_0000203 NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_assertion wasDerivedFrom befree-20140225 NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_assertion SIO_000772 8075643 NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_assertion evidence source_evidence_literature NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_assertion description "[Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP185709.RAmpWyOjQ76gpQl_ZXkpxfImKvz6Wxr9UsGfbD3vVFqrE130_provenance.