Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_assertion wasGeneratedBy ECO_0000203 NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_assertion wasDerivedFrom befree-20140225 NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_assertion SIO_000772 23288993 NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_assertion evidence source_evidence_literature NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_assertion description "[Genotyping and haplotyping analysis was performed on the known genetic loci for autosomal dominant retinitis pigmentosa (adRP) with a panel of polymorphic markers in the two families, and then mutation screening of all coding exons of the RHO gene was performed by direct sequencing of PCR-amplified DNA fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP247919.RA1CGnlqrV_Xy4h40lVA1k9j9KBGaHzV69CNegDeZnCl4130_provenance.