Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion description "[One of the major breakthroughs both in the lamin field and for this syndrome is that many of the cellular defects observed in HGPS patient cells and model systems can be restored after treatment with a class of compounds known as FTIs (farnesyltransferase inhibitors).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion evidence source_evidence_literature NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion SIO_000772 20074076 NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion wasDerivedFrom befree-20140225 NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_assertion wasGeneratedBy ECO_0000203 NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209075.RACJIYDL6PpYqJdVjKH1naRcVR3Uo_r22KNDxxHsnqNwo130_provenance.