Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_assertion description "[Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_assertion evidence source_evidence_literature NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_assertion SIO_000772 18565828 NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_assertion wasDerivedFrom gad-20150221 NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_assertion wasGeneratedBy ECO_0000203 NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.
- gad-20150221 importedOn "2015-02-21" NP124891.RAVfEfb7aFtZ80MWW3dSg6eVryPxYFzGWvS4QL5DzFu5k130_provenance.