Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.
- befree-2016 importedOn "2016-02-19" NP262858.RAsXKA3R8qo7kqw58NhXFXC53YXzUHevwkhydKUqp7ElY130_provenance.
- 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.