Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_assertion type Assertion NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_head.
- NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_assertion description "[Given that mutations in EFEMP1 have been recently described in patients with Doyne honeycomb retinal dystrophy, EFEMP2 becomes a good candidate for such disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_provenance.
- NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_assertion evidence source_evidence_literature NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_provenance.
- NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_assertion SIO_000772 10982184 NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_provenance.
- NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_assertion wasDerivedFrom befree-20150227 NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_provenance.
- NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_assertion wasGeneratedBy ECO_0000203 NP396252.RAqOs8C327TrisW61OjPqzuEV9J1UCTT2FlKjOfz6pll4130_provenance.