Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_assertion> ?p ?o ?g. }
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- NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_assertion type Assertion NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_head.
- NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_assertion description "[Based on the studies in mice, we have screened DNA from human families and identified a nonsense mutation in the human ortholog of the murine Comt2 gene that causes nonsyndromic deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_provenance.
- NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_assertion evidence source_evidence_literature NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_provenance.
- NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_assertion SIO_000772 18794526 NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_provenance.
- NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_assertion wasDerivedFrom befree-20150227 NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_provenance.
- NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_assertion wasGeneratedBy ECO_0000203 NP980439.RAtZcNukDoWm1NVQgPn6NSNrZL-K2c35SPkmxiz17cR_Y130_provenance.