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- NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_assertion type Assertion NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_head.
- NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_assertion wasGeneratedBy ECO_0000203 NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_provenance.
- NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_assertion wasDerivedFrom befree-2016 NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_provenance.
- NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_assertion SIO_000772 23024041 NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_provenance.
- NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_assertion evidence source_evidence_literature NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_provenance.
- NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_assertion description "[Mutations in planar cell polarity (PCP) genes in mice cause a variety of defects including the NTD, craniorachischisis, and sometimes SB or exencephaly (EX); they also demonstrate the role of digenic combinations of PCP mutants in NTDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016687.RAP4vOKUq2959C2ZB7KM99rahGc2Gzb0FJDvQalfFlthU130_provenance.