Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is an autosomal hereditary disorder associated with a major reduction in serum A1AT levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_assertion evidence source_evidence_literature NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_assertion SIO_000772 3289385 NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_assertion wasDerivedFrom befree-20140225 NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_assertion wasGeneratedBy ECO_0000203 NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP492679.RAx1gt1dlAY6ej0CCedVkxlN2uh-QT0AFrC97BoJwWLnE130_provenance.