Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_assertion description "[The present multiparameter analysis demonstrates the presumable direct involvement of the SP-B intron 4 deletion variant allele as a genetic risk factor to BPD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_assertion evidence source_evidence_literature NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_assertion SIO_000772 15102713 NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_assertion wasDerivedFrom befree-20150227 NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_assertion wasGeneratedBy ECO_0000203 NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP691542.RAZQ3bVhRlnflWP_74qFT4rWUdpuIxwoCyP3X8zJjQ4cY130_provenance.