Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_assertion> ?p ?o ?g. }
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- NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_assertion type Assertion NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_head.
- NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_assertion description "[The search for potential candidate genes within the 8-Mb overlapping homozygous region in these families revealed the presence of CLRN1, a gene previously known to cause Usher's syndrome type III (USH3), which was analyzed by direct sequence analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_provenance.
- NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_assertion evidence source_evidence_literature NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_provenance.
- NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_assertion SIO_000772 21310491 NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_provenance.
- NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_assertion wasDerivedFrom befree-20140225 NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_provenance.
- NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_assertion wasGeneratedBy ECO_0000203 NP513906.RAdS3qJpggoOvtFPJjP6chdLD_1W0UuX8bVq8VVedmhWc130_provenance.