Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_assertion wasGeneratedBy ECO_0000203 NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_assertion wasDerivedFrom befree-20140225 NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_assertion SIO_000772 18950394 NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_assertion evidence source_evidence_literature NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_assertion description "[In both patients, a GJB2 mutation (N14K) was identified, which shares the same gene with classic Keratitis-ichthyosis-deafness syndrome but has never been described in patients with this condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP413184.RAwIPJbwqkQotacDrkzK6_P9FS10dM22YP0G-nRaFv2VU130_provenance.