Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_assertion> ?p ?o ?g. }
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- NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_assertion type Assertion NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_head.
- NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_assertion wasGeneratedBy ECO_0000203 NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_provenance.
- NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_assertion wasDerivedFrom befree-2016 NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_provenance.
- NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_assertion SIO_000772 23024041 NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_provenance.
- NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_assertion evidence source_evidence_literature NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_provenance.
- NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_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." NP1016688.RAUnPG1OoKn6pCefZC-QMCH-n7jnRkRtWg3Qaf-fCL-1A130_provenance.