Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_assertion description "[Other markers preferentially expressed in CCRCC or PRCC, such as HIG-2, claudin 7, and EpCAM, yielded inconsistent results in Xp11 translocation RCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_assertion evidence source_evidence_literature NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_assertion SIO_000772 20679884 NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_assertion wasDerivedFrom befree-20140225 NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_assertion wasGeneratedBy ECO_0000203 NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP787257.RADishD5AaBHP6o9XR4r9_CyLdOSrtFChcXYGNdm90X4M130_provenance.