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- source_evidence_literature type ECO_0000212 NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_assertion description "[Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_assertion evidence source_evidence_literature NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_assertion SIO_000772 21857984 NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_assertion wasDerivedFrom befree-2016 NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_assertion wasGeneratedBy ECO_0000203 NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.
- befree-2016 importedOn "2016-02-19" NP918339.RAbeFfd-Zv2QrijwZX2cldCgGZeomLHqhusyYzp3F2shg130_provenance.