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- source_evidence_literature type ECO_0000212 NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_assertion description "[CHMP2B mutations are not a common cause of frontotemporal lobar degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_assertion evidence source_evidence_literature NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_assertion SIO_000772 16431024 NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_assertion wasDerivedFrom befree-2016 NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_assertion wasGeneratedBy ECO_0000203 NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.
- befree-2016 importedOn "2016-02-19" NP532435.RA9-9tWy1-qXfOz5jk-wX7zlLbBllwByAjCPi63vE0_is130_provenance.