Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_assertion wasGeneratedBy ECO_0000203 NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_assertion wasDerivedFrom befree-20140225 NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_assertion SIO_000772 7626145 NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_assertion evidence source_evidence_literature NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_assertion description "[We have previously reported the cloning of a gene that encodes a copper transporting P-type ATPase (ATP7B) which is defective in Wilson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP162488.RASs1_bOBZBvHxWzBLIwZWuI4MlGHaznGK5cAp7oSUTpI130_provenance.