Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion> ?p ?o ?g. }
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- NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion type Assertion NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_head.
- NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion description "[The demonstration that mutations in a gene previously associated with recessive Leber congenital amaurosis can also cause dominant RP illustrates the wide phenotypic variability of retinal degeneration genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_provenance.
- NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion evidence source_evidence_literature NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_provenance.
- NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion SIO_000772 18779497 NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_provenance.
- NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion wasDerivedFrom lhgdn-20090331 NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_provenance.
- NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_assertion wasGeneratedBy ECO_0000203 NP185531.RA3FNmGFPZ25ZFV8ry3QczuDExajzNT2mY7dZhCy7mB_8130_provenance.