Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion> ?p ?o ?g. }
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- NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion type Assertion NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_head.
- NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion description "[Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_provenance.
- NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion evidence source_evidence_literature NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_provenance.
- NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion SIO_000772 19247433 NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_provenance.
- NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion wasDerivedFrom befree-20150227 NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_provenance.
- NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_assertion wasGeneratedBy ECO_0000203 NP800403.RAUb0nnhZG8-MrJSbk9M6KFzEstYlu_eFFg_w9-KrSTOY130_provenance.