Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion type Assertion NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_head.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion wasGeneratedBy ECO_0000203 NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion wasDerivedFrom befree-20140225 NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion SIO_000772 21844581 NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion evidence source_evidence_literature NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.
- NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_assertion description "[Although XLG is not a rare disease, there have been no reports of PHKA2 mutations in Koreans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787292.RAk3YMDxuYkRE2RX8z__moVE0ZKqxObtxRl5S_Sqbd8Uo130_provenance.