Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_assertion description "[Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_assertion evidence source_evidence_literature NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_assertion SIO_000772 19400538 NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_assertion wasDerivedFrom befree-2016 NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_assertion wasGeneratedBy ECO_0000203 NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.
- befree-2016 importedOn "2016-02-19" NP735226.RAh0LdrWj59GPKk270JPl0WCy7iq782PS7gM8AP4XuzQk130_provenance.