Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_assertion type Assertion NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_head.
- NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_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." NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_provenance.
- NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_assertion evidence source_evidence_literature NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_provenance.
- NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_assertion SIO_000772 19068278 NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_provenance.
- NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_assertion wasDerivedFrom befree-2016 NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_provenance.
- NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_assertion wasGeneratedBy ECO_0000203 NP708215.RAzDRk5QiMXp1wmojktGuUqvmS7A6AmnvN-lCx_6hltFE130_provenance.