Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_assertion description "[A molecular case report of autosomal dominant retinitis pigmentosa: RP1/RHO sequence variants in a Turkish family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_assertion evidence source_evidence_literature NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_assertion SIO_000772 22321012 NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_assertion wasDerivedFrom befree-20150227 NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_assertion wasGeneratedBy ECO_0000203 NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP671993.RASHYSflIyg4bCpWJfnlkk7hR6JQIr3oFu199RIJ1mxcU130_provenance.