Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_assertion description "[This indicates that mutations in the USH1C gene make a greater contribution to Usher syndrome type 1 than originally thought, which has implications for the genetic testing of families with Usher syndrome in the UK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_assertion evidence source_evidence_literature NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_assertion SIO_000772 12702164 NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_assertion wasDerivedFrom befree-20140225 NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_assertion wasGeneratedBy ECO_0000203 NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651048.RAXuJTDwmauPx-2kL5nZ8UyxjwiZeGGSNyAmEzQaSCySs130_provenance.