Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_assertion description "[These findings strongly implicate defects of RDH5 as the cause of fundus albipunctatus and point to a heterogeneity of RDH5 mutations in this form of congenital stationary night blindness with variable expressivity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_assertion evidence source_evidence_literature NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_assertion SIO_000772 10617778 NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_assertion wasDerivedFrom befree-20140225 NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_assertion wasGeneratedBy ECO_0000203 NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP329243.RARUoJdQZmGxkvSo7FjmPsVGTf-xNWSrjXSp5cVj2slA8130_provenance.