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- source_evidence_literature type ECO_0000212 NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_assertion evidence source_evidence_literature NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_assertion SIO_000772 22187985 NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_assertion wasDerivedFrom befree-2016 NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_assertion wasGeneratedBy ECO_0000203 NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.
- befree-2016 importedOn "2016-02-19" NP948369.RA5dKOqJk01JPdqeURmLqGFes-GfnDHB_H9HPFHbUuUJE130_provenance.