Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_assertion type Assertion NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_head.
- NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_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." NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_provenance.
- NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_assertion evidence source_evidence_literature NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_provenance.
- NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_assertion SIO_000772 16358361 NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_provenance.
- NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_assertion wasDerivedFrom befree-20140225 NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_provenance.
- NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_assertion wasGeneratedBy ECO_0000203 NP565721.RAAGv1V1NwLXvVXnXnTElJ41gJFxb4r6I2B-jo4VnTUCE130_provenance.