Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_assertion> ?p ?o ?g. }
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- NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_assertion type Assertion NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_head.
- NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_assertion wasGeneratedBy ECO_0000203 NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_provenance.
- NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_assertion wasDerivedFrom befree-20150227 NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_provenance.
- NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_assertion SIO_000772 10484781 NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_provenance.
- NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_assertion evidence source_evidence_literature NP257122.RAEQl-UhZh7HFDNw401YvWaXlJwue55FogDIGQPJEo_tA130_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.