Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_assertion description "[To describe the mutations in the CLRN1 gene in patients from 2 consanguineous Pakistani families diagnosed with autosomal recessive retinitis pigmentosa (arRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_assertion evidence source_evidence_literature NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_assertion SIO_000772 21310491 NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_assertion wasDerivedFrom befree-20140225 NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_assertion wasGeneratedBy ECO_0000203 NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP275363.RAxEQWZZSzmmV_OCsLCLy9k27jbOxECivYn0TEDxadpzc130_provenance.