Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_assertion description "[To identify novel candidate genes for the complete form of CSNB (i.e., CSNB1) we screened the physically vast region Xp11.3-Xp11.4 for cDNA sequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_assertion evidence source_evidence_literature NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_assertion SIO_000772 10982042 NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_assertion wasDerivedFrom befree-2016 NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_assertion wasGeneratedBy ECO_0000203 NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.
- befree-2016 importedOn "2016-02-19" NP294733.RAI9TGosGu2lLQ9E3aC1uCGVQE_I_5ce12OgO1OLMXdhA130_provenance.