Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_assertion description "[In contrast to the previous definition of PCH-1, our observations suggest the existence of milder phenotypes with pontocerebellar hypoplasia or olivopontocerebellar atrophy in combination with anterior horn cell loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_assertion evidence source_evidence_literature NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_assertion SIO_000772 12548734 NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_assertion wasDerivedFrom befree-2016 NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_assertion wasGeneratedBy ECO_0000203 NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.
- befree-2016 importedOn "2016-02-19" NP381555.RAfnRQzgXzVcux3qupdzyfPM1XdmIFfFQRhu7_qCp_9cw130_provenance.