Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_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." NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_assertion evidence source_evidence_literature NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_assertion SIO_000772 9219833 NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_assertion wasDerivedFrom befree-20140225 NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_assertion wasGeneratedBy ECO_0000203 NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP607041.RAkR2GH3viHLgWb0kngOtk0IHSxqinm2zN4J_elUq0RRA130_provenance.