Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_assertion type Assertion NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_head.
- NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_assertion wasGeneratedBy ECO_0000203 NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_provenance.
- NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_assertion wasDerivedFrom befree-20140225 NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_provenance.
- NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_assertion SIO_000772 11020419 NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_provenance.
- NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_assertion evidence source_evidence_literature NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_provenance.
- NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_assertion description "[Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of leber hereditary optic neuropathy who showed marked differences in clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641331.RAOZWZGs90hMgECbeRz2uh99LtyExE_QZap5o5Tcqym14130_provenance.