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- source_evidence_literature type ECO_0000212 NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_assertion description "[To investigate the retinal disease expression in USH2C, the subtype of Usher syndrome type 2 recently shown to be caused by mutation in the VLGR1 gene, and compare results with those from USH2A, a more common cause of Usher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_assertion evidence source_evidence_literature NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_assertion SIO_000772 15671307 NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_assertion wasDerivedFrom befree-20150227 NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_assertion wasGeneratedBy ECO_0000203 NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP954493.RA1y2i2uUeKOV7NG2GpTptY-7l5MHjBrlziJEENEeuUbY130_provenance.