Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_assertion description "[We, therefore, studied genes pertinent to early embryologic development of the ANS including mammalian achaete-scute homolog-1 (MASH1), bone morphogenic protein-2 (BMP2), engrailed-1 (EN1), TLX3, endothelin converting enzyme-1 (ECE1), endothelin-1 (EDN1), PHOX2a, and PHOX2b in 67 probands with CCHS, and gender- and ethnicity-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_assertion evidence source_evidence_literature NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_assertion SIO_000772 14608649 NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_assertion wasDerivedFrom befree-20140225 NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_assertion wasGeneratedBy ECO_0000203 NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP917103.RAZwzhTMWgqXBwbt4jTdrjXpNgaVR5iUwIsKxtTe5e93s130_provenance.