Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_assertion type Assertion NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_head.
- NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_assertion description "[In addition to the Bj�rnstad syndrome, BCS1L mutations cause complex III deficiency and the GRACILE syndrome, which in neonates are lethal conditions that have multisystem and neurologic manifestations typifying severe mitochondrial disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.
- NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_assertion evidence source_evidence_literature NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.
- NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_assertion SIO_000772 17314340 NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.
- NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_assertion wasDerivedFrom befree-20140225 NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.
- NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_assertion wasGeneratedBy ECO_0000203 NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.