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- source_evidence_literature type ECO_0000212 NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_assertion description "[Clinical parameters can predict for mutation carriers and help prioritize gene testing to reduce costs in nonsyndromic pheochromocytoma presentations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_assertion evidence source_evidence_literature NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_assertion SIO_000772 19825962 NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_assertion wasDerivedFrom gad-20150221 NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_assertion wasGeneratedBy ECO_0000203 NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP157957.RADPa6LfhyDvKuJnNVkpp80SbK1oXxs1U2ke-OWSPTapc130_provenance.