Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_assertion description "[Inherited retinal degenerations such as retinitis pigmentosa (RP) are characterized by progressive loss of photoreceptors, apparently by apoptosis, and our recent report of increased secreted Frizzled-related protein-2 (SFRP2) in RP retinas suggests altered Wnt signalling may be a component of the degenerative process.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_assertion evidence source_evidence_literature NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_assertion SIO_000772 11192610 NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_assertion wasDerivedFrom befree-20140225 NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_assertion wasGeneratedBy ECO_0000203 NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP880822.RA_FkcOe9NScV90dXNGfLtVuHQppBqvdjcA4kLfaWdpEk130_provenance.