Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_assertion description "[The associated variants at the 1q21.3 locus span a region with ten genes, and plausible candidate genes for melanoma susceptibility include ARNT and SETDB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_assertion evidence source_evidence_curated NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_assertion SIO_000772 21983785 NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_assertion wasDerivedFrom ctd_human-20150221 NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_assertion wasGeneratedBy ECO_0000218 NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP7512.RAoiihpEnE_ABctd-UsFnhRduMgsygwRUR8IqV8jcpee8130_provenance.