Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_assertion> ?p ?o ?g. }
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- NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_assertion type Assertion NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_head.
- NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_assertion description "[Molecular studies have shown that besides the well-known hypomorphic recombination activating gene defects, mutations in the nonhomologous end-joining factor Artemis and in the interleukin-7 receptor alpha chain can contribute to the development of Omenn syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_provenance.
- NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_assertion evidence source_evidence_literature NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_provenance.
- NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_assertion SIO_000772 16763459 NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_provenance.
- NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_assertion wasDerivedFrom befree-20140225 NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_provenance.
- NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_assertion wasGeneratedBy ECO_0000203 NP770153.RATQ5t_TvyMEGwLfWIKmPf0Pi0RZladrodan5G7Uu3Crc130_provenance.