Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_assertion description "[In utero copper treatment for Menkes disease associated with a severe ATP7A mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_assertion evidence source_evidence_curated NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_assertion SIO_000772 22695177 NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_assertion wasDerivedFrom ctd_human-2016 NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_assertion wasGeneratedBy ECO_0000218 NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP31505.RAaAN5QfwzIFVzu2YBQy4B-zTf0xMX_RD2eJpZU5abvqU130_provenance.