Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_assertion description "[Our results strongly suggest that the clinical heterogeneity in XP-A is due to different mutations in the XPAC gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_assertion evidence source_evidence_curated NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_assertion SIO_000772 1372103 NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_assertion wasDerivedFrom uniprot-20130724 NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_assertion wasGeneratedBy ECO_0000218 NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP7135.RAwjNbcugDUfgDErU6wYAhsCFEq87ZFhz_iOA1-iqAUnc130_provenance.