Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_assertion> ?p ?o ?g. }
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- NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_assertion type Assertion NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_head.
- NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_provenance.
- NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_assertion evidence source_evidence_literature NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_provenance.
- NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_assertion SIO_000772 23304067 NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_provenance.
- NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_assertion wasDerivedFrom befree-20140225 NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_provenance.
- NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_assertion wasGeneratedBy ECO_0000203 NP313963.RAZTm_1GB_T9S_m5gTA-FSnage7k74wvZITmWOT_s6Wxs130_provenance.