Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_assertion description "[The region of genetic linkage included ATP7A, which encodes a copper-transporting P-type ATPase mutated in patients with Menkes disease, a severe infantile-onset neurodegenerative condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_assertion evidence source_evidence_literature NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_assertion SIO_000772 20170900 NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_assertion wasDerivedFrom befree-2016 NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_assertion wasGeneratedBy ECO_0000203 NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.
- befree-2016 importedOn "2016-02-19" NP794841.RABRlO2aORdbd4ic9RvEyaDQZt_8hszPH5n7kD7HX-RXI130_provenance.