Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion> ?p ?o ?g. }
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- NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion type Assertion NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_head.
- NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion description "[Diverse mutations in the gene encoding the copper transporter ATP7A lead to X-linked recessive Menkes disease or occipital horn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_provenance.
- NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion evidence source_evidence_literature NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_provenance.
- NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion SIO_000772 24754450 NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_provenance.
- NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion wasDerivedFrom befree-20150227 NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_provenance.
- NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_assertion wasGeneratedBy ECO_0000203 NP257141.RA6Wiq9gTBFH4D7eZnXro-eTFbgIXXeM8f7E0SL2fWV74130_provenance.