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- source_evidence_literature type ECO_0000212 NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_assertion description "[Additional loci and genes (OPA2, OPA6 and OPA7) are responsible for X-linked or recessive optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_assertion evidence source_evidence_literature NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_assertion SIO_000772 22776096 NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_assertion wasDerivedFrom befree-2016 NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_assertion wasGeneratedBy ECO_0000203 NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.
- befree-2016 importedOn "2016-02-19" NP996193.RACk81zu8jUusUn2w1xz0HsLV2Mo03XW7q_PE5VkoFYOg130_provenance.