Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_assertion description "[No association of chromatin-modifying protein 2B with sporadic frontotemporal dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_assertion evidence source_evidence_literature NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_assertion SIO_000772 16979267 NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_assertion wasDerivedFrom befree-2016 NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_assertion wasGeneratedBy ECO_0000203 NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.
- befree-2016 importedOn "2016-02-19" NP569579.RASi2_l8z1FnhDuBMgHVVJYpXEEI-WYZTH_B68P6MSFOU130_provenance.