Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_assertion description "[To address these issues, we genotyped SNPs in ANK3, CACNA1C, CMTM8, DGKH, EGFR, and NPAS3, which were significantly associated with BPD in previous GWAS, in a sample of 380 BPD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_assertion evidence source_evidence_literature NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_assertion SIO_000772 21654738 NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_assertion wasDerivedFrom befree-20140225 NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_assertion wasGeneratedBy ECO_0000203 NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP683562.RAOTDkODU3La8IvxY3qUbm4ObnmT2sXN6gGi-MXBbeMdQ130_provenance.