Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_assertion type Assertion NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_head.
- NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_assertion description "[Mutations in the genes encoding ATP7A and ATP7B lead to copper deficiency and toxicity disorders, Menkes and Wilson diseases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.
- NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_assertion evidence source_evidence_literature NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.
- NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_assertion SIO_000772 21242307 NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.
- NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_assertion wasDerivedFrom befree-20150227 NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.
- NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_assertion wasGeneratedBy ECO_0000203 NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.