Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_assertion description "[We assessed the frequency of SDHB, SDHC, and SDHD gene mutations by PCR amplification and sequencing in a set of head and neck paraganglioma patients who were previously managed in two otolaryngology clinics in the USA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_assertion evidence source_evidence_literature NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_assertion SIO_000772 11897817 NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_assertion wasDerivedFrom gad-20150221 NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_assertion wasGeneratedBy ECO_0000203 NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP73403.RA3gJmoDHaVMgm4OUlRLcb2hLQpn3lMnySYdU_o3Hzd_U130_provenance.