Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP724815.RAiIOEGB727JOLpna4OR5rDzoBhG_dRAsXE_XLlVM74Lg130_provenance.