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- source_evidence_literature type ECO_0000212 NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_assertion description "[These results represent the first identification of a specific genetic defect in OI and the first disease linked to a coding alteration in a Na+/Cl(-)-dependent neurotransmitter transporter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_assertion evidence source_evidence_literature NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_assertion SIO_000772 11458707 NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_assertion wasDerivedFrom befree-20150227 NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_assertion wasGeneratedBy ECO_0000203 NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP697994.RADRn5d0IbYarh-FPZTzK4Exn0c_Q-Em21qUipbIlWCeA130_provenance.