Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_assertion description "[? Despite the inconsistencies in ACF detection and characterization, several genetic and epigenetic changes common in both ACFs and CRC have been verified throughout the studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_assertion evidence source_evidence_literature NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_assertion SIO_000772 22182185 NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_assertion wasDerivedFrom befree-20150227 NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_assertion wasGeneratedBy ECO_0000203 NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP989339.RA2V2a-b5QMx6uNkhmqWdz4M73JZerB55u8ZrykhO_rv0130_provenance.