Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_assertion type Assertion NP425908.RAaHjmEFvIVQuXj1IfA4_yRcrp5BYQwFDXlBbIbKUDNow130_head.
- 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.