Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_assertion description "[To investigate EN2 for evidence of association with ASD, four single-nucleotide polymorphisms (SNPs) (rs3735653, rs1861972, rs1861973, rs2361689) that span the majority of the 8.0 kb gene were assessed by the transmission/disequilibrium test.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_assertion evidence source_evidence_curated NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_assertion SIO_000772 15024396 NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_assertion wasDerivedFrom ctd_human-20130708 NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_assertion wasGeneratedBy ECO_0000218 NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP14737.RANQCT4zLux6vFBzev8ucpR5_XNxOW6p8432Fk2tikV7s130_provenance.