Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_assertion description "[Finally, the coding region of RING1 was directly sequenced in subjects who carried haplotypes that were correlated with contrasting WG risks.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_assertion evidence source_evidence_literature NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_assertion SIO_000772 17967832 NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_assertion wasDerivedFrom befree-20140225 NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_assertion wasGeneratedBy ECO_0000203 NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.
- befree-20140225 importedOn "2014-02-25" NP425535.RA9LaVQf2wSppOGjfLcb3VaBZacjkOpHE6xsCzR3KLQis130_provenance.