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- NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_assertion type Assertion NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_head.
- NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_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." NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_provenance.
- NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_assertion evidence source_evidence_literature NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_provenance.
- NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_assertion SIO_000772 19247433 NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_provenance.
- NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_assertion wasDerivedFrom befree-20150227 NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_provenance.
- NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_assertion wasGeneratedBy ECO_0000203 NP723239.RAZ5H7dHqgGH-WwjY3CsBVnjZMtoNlmTj15Z6Psx2fAa4130_provenance.