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- source_evidence_literature type ECO_0000212 NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_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." NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_assertion evidence source_evidence_literature NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_assertion SIO_000772 15102713 NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_assertion wasDerivedFrom gad-20150221 NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_assertion wasGeneratedBy ECO_0000203 NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP85146.RA9k9ashD1-A4B4hg6_CPN9NTpAnKEF60xGQxDn8wC3_0130_provenance.