Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance.
- NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_assertion description "[We performed chip-based matrix-assisted laser desorption/ionisation time-of-flight (MALDI-TOF) mass spectrometry using the MassARRAY system and multiplexed genotyping assays to investigate the association between 10 single nucleotide polymorphisms (SNPs) in the ADAM33 gene (F_+1, Q_-1, S_1, ST_+4, ST_+7, V_-2, V_-1, V_2, V_4, V_5) and asthma and asthma severity in a large Australian Caucasian population of nonasthmatic controls (n = 473), and patients with mild (n = 292), moderate (n = 238) and severe (n = 82) asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance.
- NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_assertion evidence source_evidence_literature NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance.
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- NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_assertion wasDerivedFrom befree-20140225 NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance.
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- befree-20140225 importedOn "2014-02-25" NP788519.RANfSNLZmxFD0bg32lRBvlBwQjiEH6FUkPy1c5awklEFk130_provenance.