Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_assertion description "[In this article, we identify a gene, SLC39A4, located in the candidate region and, in patients with AE, document mutations that likely lead to the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_assertion evidence source_evidence_curated NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_assertion SIO_000772 12032886 NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_assertion wasDerivedFrom uniprot-20150221 NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_assertion wasGeneratedBy ECO_0000218 NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP3885.RAwgdjWrZ4TpcOm4_CF1Jv8m0x-9gYviMuux8LaSPqzME130_provenance.