Matches in Nanopublications for { ?s ?p "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 12 of
12
with 100 items per page.
- NP297058.RARC-AXIiaDQ34DzolB2M84VrXM-5C2RdKQVhwwSAptm4130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297058.RARC-AXIiaDQ34DzolB2M84VrXM-5C2RdKQVhwwSAptm4130_provenance.
- NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP156665.RAy17xueCuMKQPcPXSQasFdVZ2LH8JHn5ZYm1VH_CgKnY130_provenance.
- NP473859.RAUXHqdmijqz8YaK8faDHuN1sBU8QHrCgDE9XdcoxCUnk130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473859.RAUXHqdmijqz8YaK8faDHuN1sBU8QHrCgDE9XdcoxCUnk130_provenance.
- NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP386794.RAPhRlxj1Cj51lL_kEUyQHtVY-0ktUL4AzHNBKRSZLY7U130_provenance.
- assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755132.RAY_D0nP4K8VvgGiygnjqsYetAk2r8G3g7vZIjOZfAVQ8130_provenance.
- assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941120.RAi7ACfYq0V-250oAIm2rlffHj7uo4WZTWagrO0U-8xFQ130_provenance.
- NP941122.RAk-G7O1-vtdHd__0luZr6LCimume81D9EEnPkccT9E7g130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP941122.RAk-G7O1-vtdHd__0luZr6LCimume81D9EEnPkccT9E7g130_provenance.
- NP755133.RAj4kbS7FA3qknHFEW0pdCa-VqSRXPlIgLoNuhMqrFGFk130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755133.RAj4kbS7FA3qknHFEW0pdCa-VqSRXPlIgLoNuhMqrFGFk130_provenance.
- NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755135.RAoar37hIYZXdL9ISdW3bm1fzmU4f9C-_8aTEEq3f9K18130_provenance.
- NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_assertion description "[The phenotypes associated with mutations in NTRK1 and WNK1/HSN2 typically consisted of congenital insensitivity to pain and anhidrosis, and early-onset ulcero-mutilating sensory neuropathy, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599675.RA5B6blTRrCCmhIfiGlh1pDs4R5Eq0hdJPkrOuBdebf7k130_provenance.