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- source_evidence_literature type ECO_0000212 NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP257229.RAnV_cwwhETn1TIpoRx-G2g6oE3IPPB4YFxHaNCxljFFY130_provenance.