Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_assertion> ?p ?o ?g. }
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- NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_assertion type Assertion NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_head.
- NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_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." NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_provenance.
- NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_assertion evidence source_evidence_literature NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_provenance.
- NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_assertion SIO_000772 21840926 NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_provenance.
- NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_assertion wasDerivedFrom befree-20150227 NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_provenance.
- NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_assertion wasGeneratedBy ECO_0000203 NP639628.RAaNQGZJCJQmmfop5uJA84bnlGG8sVEGz2Qt-jW3Ztkrc130_provenance.