Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_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." NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_assertion evidence source_evidence_literature NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_assertion SIO_000772 11192610 NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_assertion wasDerivedFrom befree-20150227 NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_assertion wasGeneratedBy ECO_0000203 NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP691122.RAOPfwILB_KEd3UQCPySKl9K3o_lY18P54UG6WqkDhJGk130_provenance.