Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_assertion> ?p ?o ?g. }
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- NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_assertion type Assertion NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_head.
- NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_provenance.
- NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_assertion evidence source_evidence_literature NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_provenance.
- NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_assertion SIO_000772 10852374 NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_provenance.
- NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_assertion wasDerivedFrom befree-2016 NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_provenance.
- NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_assertion wasGeneratedBy ECO_0000203 NP286411.RAwC8yTgGtnYx7CW99G1hxkHYH5JrRpv_TBAeUKvwMLtk130_provenance.