Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_assertion type Assertion NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_head.
- NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_assertion description "[We designed a custom resequencing chip that can detect known and new sequence changes in 90 retinal disease genes using a new high-throughput strategy with a high sensitivity and specificity for one tenth of the cost of conventional direct sequencing. The]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_provenance.
- NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_assertion evidence source_evidence_literature NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_provenance.
- NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_assertion SIO_000772 20801516 NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_provenance.
- NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_assertion wasDerivedFrom gad-20150221 NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_provenance.
- NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_assertion wasGeneratedBy ECO_0000203 NP184671.RAdocoofsa9fpmhP3nFuGzcGSnUn2io7IafjOpQhm-9Ww130_provenance.