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- NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_assertion type Assertion NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_head.
- NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_assertion description "[Here, we examined ATR-pathway function in cell lines from three haploinsufficient contiguous gene-deletion disorders--a subset of blepharophimosis-ptosis-epicanthus inversus syndrome, Miller-Dieker lissencephaly syndrome, and Williams-Beuren syndrome--in which the deleted region encompasses ATR, RPA1, and RFC2, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_provenance.
- NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_assertion evidence source_evidence_literature NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_provenance.
- NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_assertion SIO_000772 17564965 NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_provenance.
- NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_assertion wasDerivedFrom befree-20140225 NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_provenance.
- NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_assertion wasGeneratedBy ECO_0000203 NP474132.RABr5xF2oOx4eliHsPD61gL1zqanvS2p9R_3jkd57m11Y130_provenance.