Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_assertion type Assertion NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_head.
- NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_assertion description "[Homozygous disruption of PCP genes in mice results in a spectrum of NTDs, including defects that affect the entire neural axis (craniorachischisis), cranial NTDs (exencephaly) and spina bifida.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_provenance.
- NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_assertion evidence source_evidence_literature NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_provenance.
- NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_assertion SIO_000772 21840926 NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_provenance.
- NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_assertion wasDerivedFrom befree-20150227 NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_provenance.
- NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_assertion wasGeneratedBy ECO_0000203 NP639631.RADhd-pieNFEJuJ7z3ZSWRDhsYnnt-4d0Qxu6vqEJKUw8130_provenance.