Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_assertion> ?p ?o ?g. }
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- NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_assertion type Assertion NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_head.
- NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_assertion description "[Comparison of this patient's dysmorphic features with previously reported cases of ring 3 or deletion 3p suggests a clinical syndrome derived mainly from deletion of 3p26 leads to pter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_provenance.
- NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_assertion evidence source_evidence_literature NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_provenance.
- NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_assertion SIO_000772 7154048 NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_provenance.
- NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_assertion wasDerivedFrom befree-2016 NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_provenance.
- NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_assertion wasGeneratedBy ECO_0000203 NP1307724.RAOPUwlswb905meJErIz5NM4EHKemIcDjb76PQWnfFmOU130_provenance.