Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_assertion description "[Blood was taken from the proband and his parents, genomic DNA was isolated and some candidate genes for cataract (CRYAA, CRYBB2, GJA8) or macular hypoplasia (OA1, P) or both (PAX6) were analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_assertion evidence source_evidence_literature NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_assertion SIO_000772 16453125 NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_assertion wasDerivedFrom befree-20150227 NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_assertion wasGeneratedBy ECO_0000203 NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP328425.RACH19UH54Dx3JBXObxqfabTPPDMhqxmr0s0NrG1mES8w130_provenance.