Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_assertion> ?p ?o ?g. }
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- NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_assertion type Assertion NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_head.
- NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_assertion wasGeneratedBy ECO_0000203 NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.
- NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_assertion wasDerivedFrom befree-2016 NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.
- NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_assertion SIO_000772 10484781 NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.
- NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_assertion evidence source_evidence_literature NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_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.