Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_assertion description "[Mutation of acceptor splice site of the SEDL gene in X-linked spondyloepiphyseal dysplasia tarda causes the activation of cryptic splice site.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_assertion evidence source_evidence_literature NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_assertion SIO_000772 15952107 NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_assertion wasDerivedFrom befree-2016 NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_assertion wasGeneratedBy ECO_0000203 NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.
- befree-2016 importedOn "2016-02-19" NP499170.RAYP9li7NDOglSmUxQ98WiU8_oKtRH1EaAJniJDV8Gdho130_provenance.