Matches in Nanopublications for { ?s ?p "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP245001.RAN01mePEaxNFIMULTDpuocsv7OPAIYMcRqJOqLAIdi0g130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245001.RAN01mePEaxNFIMULTDpuocsv7OPAIYMcRqJOqLAIdi0g130_provenance.
- NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519468.RAAFlKNbbbZzCdEGbECa44rr7aJckNgRHU8zuarqD--zk130_provenance.
- assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP408549.RAQJhtP3SsHWjAXUEO0Ytj7p1YF_9aM9XeTEab49qeGkE130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408549.RAQJhtP3SsHWjAXUEO0Ytj7p1YF_9aM9XeTEab49qeGkE130_provenance.
- NP408548.RAKq7auo9HRrLU1mRrJfslqSA4Y7_j_n9p2efak3jGnfA130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408548.RAKq7auo9HRrLU1mRrJfslqSA4Y7_j_n9p2efak3jGnfA130_provenance.
- NP408553.RAEWGTwg-JFMIHrRmeJs3BzM4iBs4BEBNTuSKk7hc5gbg130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408553.RAEWGTwg-JFMIHrRmeJs3BzM4iBs4BEBNTuSKk7hc5gbg130_provenance.
- NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_assertion description "[Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHP1B) have an imprinting defect of the G(s)alpha gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific G(s)alpha deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408556.RA6w3044kft1I1Kl7HYZ-Kpc_wxnYz3uFlIgvND0IkfOw130_provenance.