Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion type Assertion NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_head.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion description "[This is the second report of LCA5 mutations causing Leber congenital amaurosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion evidence source_evidence_literature NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion SIO_000772 18334959 NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion wasDerivedFrom lhgdn-20090331 NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.
- NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_assertion wasGeneratedBy ECO_0000203 NP122357.RARE-7QangkKTXkT9Xb75AyJrabgB2WwFHlrL7lmqMfLs130_provenance.