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- source_evidence_literature type ECO_0000212 NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_assertion description "[Interestingly, mutations of connexin genes have been reported in several human diseases (peripheral neuropathies, cardiovascular and dermatological diseases, hereditary cataract, and deafness) and altered expression of connexins have been associated with tumoral progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_assertion evidence source_evidence_literature NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_assertion SIO_000772 16677845 NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_assertion wasDerivedFrom befree-20140225 NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_assertion wasGeneratedBy ECO_0000203 NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485355.RAno4-Sk0VNwX-JUWqfXkzzgSrpkmMDAQJVDPxW1_vTJU130_provenance.