Matches in Nanopublications for { ?s ?p "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP428337.RAUZViEPSbck5CNEhkso7_Qy14908uYACQokuM6BLSk1M130_assertion description "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428337.RAUZViEPSbck5CNEhkso7_Qy14908uYACQokuM6BLSk1M130_provenance.
- NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_assertion description "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- NP418439.RAM3SOQVgpf6jI68zeU47_UlGe_8eJcYnl0CkVgxDPZKI130_assertion description "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418439.RAM3SOQVgpf6jI68zeU47_UlGe_8eJcYnl0CkVgxDPZKI130_provenance.
- NP418440.RA37JoM_tzG5aoOTC4vkk90fPPjO3fUePm2NdkTtWuYcY130_assertion description "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418440.RA37JoM_tzG5aoOTC4vkk90fPPjO3fUePm2NdkTtWuYcY130_provenance.