Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- befree-20150227 importedOn "2015-02-27" NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_assertion wasGeneratedBy ECO_0000203 NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_assertion wasDerivedFrom befree-20150227 NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_assertion SIO_000772 24281366 NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_assertion evidence source_evidence_literature NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.
- NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_assertion description "[Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_provenance.