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- source_evidence_literature type ECO_0000212 NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_assertion description "[Remarkably, careful review of the clinical data showed that mutations in RPL5 are associated with multiple physical abnormalities, including craniofacial, thumb, and heart anomalies, whereas isolated thumb malformations are predominantly present in patients carrying mutations in RPL11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_assertion evidence source_evidence_literature NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_assertion SIO_000772 19061985 NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_assertion wasDerivedFrom befree-20150227 NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_assertion wasGeneratedBy ECO_0000203 NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.
- befree-20150227 importedOn "2015-02-27" NP675088.RAKWwRr8csaztGvhB8CvN-eGYhw1NGTSE5OCjDukl1L30130_provenance.