Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_assertion description "[Our results are consistent with a loss of alleles on 17p in 50% of CNS PNETs, but do not suggest that PEDF is a candidate for the PNET suppressor gene in 17p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_assertion evidence source_evidence_literature NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_assertion SIO_000772 9219833 NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_assertion wasDerivedFrom befree-20150227 NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_assertion wasGeneratedBy ECO_0000203 NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP615803.RAPUqa68IiIFd-oZl2Q_KIdBo8xm2VeNWURS7MUoWEQ6o130_provenance.