Matches in Nanopublications for { ?s ?p "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575732.RAcdArlk8_49FkY9IjaFZuipXyqJwpusN5WJH3Z6okrY4130_provenance.
- NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_provenance.
- NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_provenance.
- assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP722933.RAWZ6vKz2keXD5A_8fF0-WvVBpQw-YeFo64BPhY9cgAp0130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722933.RAWZ6vKz2keXD5A_8fF0-WvVBpQw-YeFo64BPhY9cgAp0130_provenance.
- NP723507.RAmdi-qZPuGVkTLfY-K9EGeexV7vuLFeWeIxTmbtXRdq0130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723507.RAmdi-qZPuGVkTLfY-K9EGeexV7vuLFeWeIxTmbtXRdq0130_provenance.
- NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800418.RA4XLnQ1v6qPPOL_kILc2MLewajBPBhA0FLbg2S-MKMEA130_provenance.
- NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722932.RA40tfKNx-9hzh8jMtqDcEUs5ybHOkqP8aVZFcCR_GpNs130_provenance.
- NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722934.RA1xIRsjKhcqhm1z_96dQdRbYaW_T6fBAmJNaquY_k_9A130_provenance.
- NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722936.RA63ZDcfTvPO1GgxEhxS5OMx2xUL88Lavn1eIJzdaMx8E130_provenance.