Matches in Nanopublications for { ?s ?p "[Menkes disease is an X-linked recessive copper deficiency disorder caused by mutations in the ATP7A ( MNK ) gene which encodes a copper transporting P-type ATPase (MNK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Menkes disease is an X-linked recessive copper deficiency disorder caused by mutations in the ATP7A ( MNK ) gene which encodes a copper transporting P-type ATPase (MNK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP262859.RA-mze6pTuz1dkJ8gmpbMmSLqE43iLbEejKGGfTnfZPlg130_assertion description "[Menkes disease is an X-linked recessive copper deficiency disorder caused by mutations in the ATP7A ( MNK ) gene which encodes a copper transporting P-type ATPase (MNK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262859.RA-mze6pTuz1dkJ8gmpbMmSLqE43iLbEejKGGfTnfZPlg130_provenance.
- NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_assertion description "[Menkes disease is an X-linked recessive copper deficiency disorder caused by mutations in the ATP7A ( MNK ) gene which encodes a copper transporting P-type ATPase (MNK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_provenance.
- NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_assertion description "[Menkes disease is an X-linked recessive copper deficiency disorder caused by mutations in the ATP7A ( MNK ) gene which encodes a copper transporting P-type ATPase (MNK).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.