Matches in Nanopublications for { ?s ?p "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7065.RATF535Z7vUEG8816xUJuQsTsRGZ7iBP9gFcyaw8zDZZo130_provenance.
- NP33757.RAZ9yr__dG_VedqxP6cElGaGaeLtjxGizdNNcBm88-tzw130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33757.RAZ9yr__dG_VedqxP6cElGaGaeLtjxGizdNNcBm88-tzw130_provenance.
- assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP34302.RAA9WgAmamSVamQbU61GVFBJiEiX_BABsW7HTwb1lKelM130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP34302.RAA9WgAmamSVamQbU61GVFBJiEiX_BABsW7HTwb1lKelM130_provenance.
- NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_provenance.
- NP26794.RAlDE4_1JfwQXewEm3azsYgNwarmUim-CvRMc_8kbdBiA130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26794.RAlDE4_1JfwQXewEm3azsYgNwarmUim-CvRMc_8kbdBiA130_provenance.
- NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6349.RAFRr6k49mKC53NjFLgYJpBjM2QgBIDyo1FpiP-bTLoAo130_provenance.
- NP837147.RAKBqYVZCMfDyTt-EUw2blOp_OguA_HW10kNX4MAN3r3A130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837147.RAKBqYVZCMfDyTt-EUw2blOp_OguA_HW10kNX4MAN3r3A130_provenance.