Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_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." NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_assertion evidence source_evidence_literature NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_assertion SIO_000772 9219833 NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_assertion wasDerivedFrom befree-2016 NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_assertion wasGeneratedBy ECO_0000203 NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1376657.RAL-t8CTiHSUrOOtb-h8OzjPq-2ZwzyRZLtBaQq6G3OEI130_provenance.