Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_assertion description "[Recently, the same FGFR3 mutations known from skeletal dysplasia syndromes and urothelial carcinoma have been shown to cause benign human skin tumors such as seborrheic keratoses and epidermal nevi.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_assertion evidence source_evidence_literature NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_assertion SIO_000772 17172848 NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_assertion wasDerivedFrom befree-20140225 NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_assertion wasGeneratedBy ECO_0000203 NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP157778.RAJdWtzCMNpN24ayrJXFifasl9LlQdZMieSRMMMEp16Xg130_provenance.