Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP516632.RAVPG8CdpBjpum3nxFrINh7VVXu25klWXdLsFovJ3fw10130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516632.RAVPG8CdpBjpum3nxFrINh7VVXu25klWXdLsFovJ3fw10130_provenance.
• NP578054.RAWg9yglrcZ6bH1JHHphlsA3AHINNZ3unFu-mJTerdIco130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578054.RAWg9yglrcZ6bH1JHHphlsA3AHINNZ3unFu-mJTerdIco130_provenance.
• NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370038.RAghOMFIa1RSwd7LTq5uVAsHkmUQ8HVCkeMgimvqi5H8g130_provenance.
• NP371850.RAcOJBzOghTtLpQC9krBk1eM5Md9aKZwzNjLAKmEOmXoQ130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371850.RAcOJBzOghTtLpQC9krBk1eM5Md9aKZwzNjLAKmEOmXoQ130_provenance.
• NP717748.RAolIX5Cmk-LF2_Mr3UABMLTCz-OO6HZfmNEFqkT8urJI130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717748.RAolIX5Cmk-LF2_Mr3UABMLTCz-OO6HZfmNEFqkT8urJI130_provenance.
• NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469966.RAuCu8livO5zdshkypdgsdX2oiLaTkiwoYRLto_tx0XvY130_provenance.
• NP558727.RAsg8Axzl6h8tOzABwLV92yYQ2x_S_YVOa_S2y-MdybT8130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558727.RAsg8Axzl6h8tOzABwLV92yYQ2x_S_YVOa_S2y-MdybT8130_provenance.
• NP558705.RARTMTN-KJ__mLO7vzu8DJpTZM64yX6K-nDjiJb3GolSU130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558705.RARTMTN-KJ__mLO7vzu8DJpTZM64yX6K-nDjiJb3GolSU130_provenance.
• NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798624.RA9yJ0jswt_bgOx-zQDVT2pe1DIWXL2usZy-3VEbx_TLw130_provenance.
• NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883060.RA0m5Wkq0bLoQvm64z0lD9oC3YDkK0XfXi88ZinSPzdGU130_provenance.
• NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266339.RA_X1_kAObx1RT9eb9CK3uo20E5AZT5kWmQjIZNEiTWLY130_provenance.
• NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600176.RA4k6KzAVa2FJwWsLrghq52OZcPTUL7GpvQLVxKzbcWLE130_provenance.
• NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_provenance.
• NP1361381.RAKKYWse0dkBMZd_fPd5zR2e5zc6V_Me05-ZxqRVP2td4130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1361381.RAKKYWse0dkBMZd_fPd5zR2e5zc6V_Me05-ZxqRVP2td4130_provenance.
• NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1361382.RAwoMRdCBLYOTtMEt2_JupK53ZkWO41waGsw5T8VYm5X8130_provenance.