Matches in Nanopublications for { ?s ?p "[A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP3127.RATIIEyIPVB9hSWjvDZRYtfMnL1O_YLLf2yTkMJAvA_bI130_assertion description "[A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3127.RATIIEyIPVB9hSWjvDZRYtfMnL1O_YLLf2yTkMJAvA_bI130_provenance.
- NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_assertion description "[A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258.RAwB5g1AHoymilrqL8iKxRQeS2ZtOTHNBFe3bw1qnXhpw130_provenance.
- assertion description "[A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_assertion description "[A novel missense mutation affecting the human hairless thyroid receptor interacting domain 2 causes congenital atrichia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2349.RArd9OwCXYDLuVPMfDRt35bhOJnqNFxHnj1kFFAob9z7I130_provenance.