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- source_evidence_literature type ECO_0000212 NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_assertion description "[BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Bj�rnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_assertion evidence source_evidence_literature NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_assertion SIO_000772 17314340 NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_assertion wasDerivedFrom befree-20150227 NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_assertion wasGeneratedBy ECO_0000203 NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP265954.RAucaQPrAazujH9CquUOMJ6j705j618TsO7MKuonQgqZ4130_provenance.