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- NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_assertion type Assertion NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_head.
- NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_assertion description "[Here we report a SCID associated with microcephaly caused by compound heterozygous hypomorphic mutations in Lig4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_provenance.
- NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_assertion evidence source_evidence_literature NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_provenance.
- NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_assertion SIO_000772 16358361 NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_provenance.
- NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_assertion wasDerivedFrom befree-20150227 NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_provenance.
- NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_assertion wasGeneratedBy ECO_0000203 NP939185.RAndSnDSOuHvGRrpDUdxeLqD419HKsoLr85nXrfneIn68130_provenance.