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- source_evidence_literature type ECO_0000212 NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_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." NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_assertion evidence source_evidence_literature NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_assertion SIO_000772 21654738 NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_assertion wasDerivedFrom befree-20150227 NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_assertion wasGeneratedBy ECO_0000203 NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936861.RAXH-s8lqG4rgXf0Acm8BtfgM_gwK5JGJoJW-Kx4_eQH0130_provenance.