Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_assertion description "[The presence of TNFRSF1A shedding defects and low sTNFRSF1A levels in 3 families without a TNFRSF1A mutation indicates that the genetic basis among patients with `TRAPS-like` features is heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_assertion evidence source_evidence_curated NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_assertion SIO_000772 13130484 NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_assertion wasDerivedFrom uniprot-20130724 NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_assertion wasGeneratedBy ECO_0000218 NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6645.RAQF6aJVJxXsrFGx3dxMaGX93rYYxJNF1In58dkF-rSBc130_provenance.