Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_assertion> ?p ?o ?g. }
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- NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_assertion type Assertion NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_head.
- NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_assertion description "[Recently, the RS1 gene underlying this common cause of early vision loss was identified and shown to encode a 224-amino acid precursor protein including a 23-residue leader sequence as well as a highly conserved discoidin motif at the C-terminus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_provenance.
- NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_assertion evidence source_evidence_literature NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_provenance.
- NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_assertion SIO_000772 10051329 NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_provenance.
- NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_assertion wasDerivedFrom befree-2016 NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_provenance.
- NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_assertion wasGeneratedBy ECO_0000203 NP246747.RAXXpvPC7h_OwzjDCQ4Y16yejXnO512QGBEOXFJZwOYKk130_provenance.