Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion> ?p ?o ?g. }
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- NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion type Assertion NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_head.
- NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion description "[We identified two unrelated individuals with a complex cranial, cervical, auricular, and skeletal malformation syndrome with scapular and pelvic hypoplasia (Cousin syndrome) that recapitulates the dysmorphic phenotype seen in the Tbx15-deficient mice, droopy ear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_provenance.
- NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion evidence source_evidence_literature NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_provenance.
- NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion SIO_000772 19068278 NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_provenance.
- NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion wasDerivedFrom befree-20150227 NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_provenance.
- NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_assertion wasGeneratedBy ECO_0000203 NP724206.RA4w3wAqzBul6XZcAWB3y8eENEFZqOAbQ9u1k1aUBASR4130_provenance.