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- NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_assertion type Assertion NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_head.
- NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_assertion description "[Twelve other patients (21 %) carried mutations in SPINT2, and were phenotypically characterized by systematic association with keratitis (p < 10(-4)) and, for half of them, with choanal atresia (p < 10(-4)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_provenance.
- NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_assertion evidence source_evidence_literature NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_provenance.
- NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_assertion SIO_000772 24142340 NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_provenance.
- NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_assertion wasDerivedFrom befree-20150227 NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_provenance.
- NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_assertion wasGeneratedBy ECO_0000203 NP849629.RAWSRxguBdiMgvPLNM3d4MIVBH1xffFT8Yupn89IK25u4130_provenance.