Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_assertion description "[The loss of Cecr2, which encodes a chromatin remodeling protein, has been associated with the neural tube defect (NTD) exencephaly and open eyelids in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_assertion evidence source_evidence_literature NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_assertion SIO_000772 21246654 NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_assertion wasDerivedFrom befree-20150227 NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_assertion wasGeneratedBy ECO_0000203 NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.
- befree-20150227 importedOn "2015-02-27" NP890544.RAKZ28klIHQEYENleDyPvN4lixbs-V__cwzI6doSb_Eys130_provenance.