Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_assertion description "[PINK1 was absent in cortical Lewy bodies, in neurofibrillary tangles in Alzheimer's disease, progressive supranuclear palsy and corticobasal degeneration, and in the glial and neuronal alpha-synuclein positive inclusions in multiple system atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_assertion evidence source_evidence_literature NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_assertion SIO_000772 16702191 NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_assertion wasDerivedFrom befree-20140225 NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_assertion wasGeneratedBy ECO_0000203 NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP647249.RAQbiyj3PfIlg21mm_QNtC6oSibX6L2dHHn-QKCG4XKFc130_provenance.