Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- befree-2016 importedOn "2016-02-19" NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_assertion wasGeneratedBy ECO_0000203 NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_assertion wasDerivedFrom befree-2016 NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_assertion SIO_000772 10409426 NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_assertion evidence source_evidence_literature NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.
- NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_assertion description "[Since mutations in unconventional myosins are known to cause several human diseases, and since mutations of unconventional myosin VIIa cause retinal degeneration, we evaluated myosin IXA as a candidate for BBS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258003.RA-47w7654ljMU_t7o-WDXM5dKWi1Ik5P-9chLO_F6Pp0130_provenance.