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- source_evidence_literature type ECO_0000212 NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_assertion description "[Mutations in KVLQT1 and KCNE1 also cause the Jervell and Lange-Nielsen syndrome, a form of LQTS associated with deafness, a phenotypic abnormality inherited in an autosomal recessive fashion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_assertion evidence source_evidence_literature NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_assertion SIO_000772 10973849 NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_assertion wasDerivedFrom befree-20150227 NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_assertion wasGeneratedBy ECO_0000203 NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP521584.RAE_wobPz0_U8kfABZYyXbwd6NijAYONXpKBs53ayonJE130_provenance.