Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_assertion> ?p ?o ?g. }
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- NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_assertion type Assertion NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_head.
- NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_assertion description "[An MKS-like incipient congenic group (F6 to F10) manifested very variable neurological features (including exencephaly, and frontal/occipital encephalocele) that were associated with the loss of primary cilia, diminished Shh signalling and dorsalization of the caudal neural tube.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_provenance.
- NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_assertion evidence source_evidence_literature NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_provenance.
- NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_assertion SIO_000772 23283079 NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_provenance.
- NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_assertion wasDerivedFrom befree-20140225 NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_provenance.
- NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_assertion wasGeneratedBy ECO_0000203 NP511612.RASfStXJdP_SugGJhJ_FCa1FfgWGQepNS_Btvak_9Fo5s130_provenance.