Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP358291.RAdWqhrN-lisGon88FO50bftDU4xJYBguzK_7--nx3Lzg130_provenance.