Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_assertion description "[Here we expand the role of GRN in FTLD-U and demonstrate that a common genetic variant (rs5848), located in the 3'-untranslated region (UTR) of GRN in a binding-site for miR-659, is a major susceptibility factor for FTLD-U.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_assertion evidence source_evidence_literature NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_assertion SIO_000772 18723524 NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_assertion wasDerivedFrom befree-20140225 NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_assertion wasGeneratedBy ECO_0000203 NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP175779.RAWbSvq2uwgBiuCtL4p4p74Q0n-xM8JUPjtDnhvNgeH8k130_provenance.