Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_assertion> ?p ?o ?g. }
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- NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_assertion type Assertion NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_head.
- NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_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." NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_provenance.
- NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_assertion evidence source_evidence_literature NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_provenance.
- NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_assertion SIO_000772 21840926 NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_provenance.
- NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_assertion wasDerivedFrom befree-20140225 NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_provenance.
- NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_assertion wasGeneratedBy ECO_0000203 NP486513.RAiQ4dd2tSf3tc-zamqmaI8MdyaUS3s_4E0mu2Ll5XVf8130_provenance.