Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_assertion description "[We studied the RET, GDNF, GFRA1, PHOX2A, PHOX2B, HASH-1, EDN1, EDN3, EDNRB, and BDNF genes in seven patients with isolated CCHS and three patients with HSCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_assertion evidence source_evidence_literature NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_assertion SIO_000772 14566559 NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_assertion wasDerivedFrom befree-20140225 NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_assertion wasGeneratedBy ECO_0000203 NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925827.RA9TC0s8OvvQsaqOUW4gvwFoYrnAKXaAV5u8h6cg-qGBA130_provenance.