Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_assertion description "[Mutations in BANF1 have been recently reported to cause a new hereditary progeroid syndrome that we now propose to call the N�stor-Guillermo progeria syndrome (NGPS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_assertion evidence source_evidence_literature NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_assertion SIO_000772 21932319 NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_assertion wasDerivedFrom befree-20140225 NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_assertion wasGeneratedBy ECO_0000203 NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP304176.RAWx0p5B6-kp1cN8zw7itAuCb6132jdPwlnSe0khXuBHI130_provenance.