Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_assertion description "[The results underlined the importance of considering the complete DNA sequencing of the SLC26A4 gene for differential molecular diagnosis of deafness, especially in those patients affected by congenital, progressive and fluctuating mixed hearing loss with bilateral EVA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_assertion evidence source_evidence_literature NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_assertion SIO_000772 22717225 NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_assertion wasDerivedFrom befree-20140225 NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_assertion wasGeneratedBy ECO_0000203 NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP311754.RA0bBZtPK8IjOAoVb8m9dglTJr_DShpNMXHtDoHljJfCY130_provenance.