Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_assertion type Assertion NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_head.
- NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_assertion wasGeneratedBy ECO_0000203 NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.
- NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_assertion wasDerivedFrom befree-20140225 NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.
- NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_assertion SIO_000772 22310223 NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.
- NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_assertion evidence source_evidence_literature NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.
- NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_assertion description "[Clinical molecular diagnostic centers routinely screen SHH, ZIC2, SIX3 and TGIF for mutations that can help to explain holoprosencephaly and related brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.