Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_assertion description "[Despite the fact that the frequency of TMIE variants in our study subjects was low, we suggested that c.257G>A (p.R86Q) variant is a de novo and may be as a risk factor for the development of hearing loss in Taiwanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_assertion evidence source_evidence_literature NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_assertion SIO_000772 20206386 NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_assertion wasDerivedFrom gad-20150221 NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_assertion wasGeneratedBy ECO_0000203 NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140854.RA_6vQvQaA3cDQWsBqkCabqyKwRiB9Vs5q46A6rNY6XJk130_provenance.