Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_assertion description "[Mutations of the RET, GFRA1, PHOX2A, and HASH-1 genes may also be involved in the pathogenesis of CCHS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_assertion evidence source_evidence_curated NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_assertion SIO_000772 14566559 NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_assertion wasDerivedFrom uniprot-2016 NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_assertion wasGeneratedBy ECO_0000218 NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP3056.RAOojhc2NPG3W1x18Zn4axC-nRmpBWHkLyb9x0o-2t1lc130_provenance.