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- source_evidence_literature type ECO_0000212 NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_assertion description "[These studies open up the possibility that all PH1 mutations, which segregate with the minor allele, might also lead to the peroxisome-to-mitochondrion mistargeting of AGT, a suggestion that has important implications for the development of treatment strategies for PH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_assertion evidence source_evidence_literature NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_assertion SIO_000772 23229545 NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_assertion wasDerivedFrom befree-20150227 NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_assertion wasGeneratedBy ECO_0000203 NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP230811.RAsPuHmaHMFaGHG1OR7U272ox4tiYgZn216Lpon1uyl_8130_provenance.