Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_assertion description "[We localized the gene for dNT-2 on chromosome 17p11.2 in the Smith-Magenis syndrome-critical region, raising the possibility that dNT-2 is involved in the etiology of this genetic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_assertion evidence source_evidence_literature NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_assertion SIO_000772 10899995 NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_assertion wasDerivedFrom befree-2016 NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_assertion wasGeneratedBy ECO_0000203 NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.
- befree-2016 importedOn "2016-02-19" NP289374.RAZsCwMbbmEGz80Lm_Tir2VRaQWfNM2JVW92avKHYT5TI130_provenance.