Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_assertion description "[We recently identified the paired-like homeobox 2B (PHOX2B) gene as the major disease-causing gene in isolated and syndromic CCHS, which prompted us to regard it as a candidate gene in NB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_assertion evidence source_evidence_literature NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_assertion SIO_000772 15024693 NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_assertion wasDerivedFrom befree-2016 NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_assertion wasGeneratedBy ECO_0000203 NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.
- befree-2016 importedOn "2016-02-19" NP435800.RAJPE4deXj3Q3a8WYtahEJBO4lBWzu7an5MNJh0H8MnVw130_provenance.