Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_assertion description "[Overall, we found 9 (13.8%) large genomic deletions or duplications: 7 out of 45 CRC patients with family history and 2 out of 20 young CRC patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_assertion evidence source_evidence_literature NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_assertion SIO_000772 15949572 NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_assertion wasDerivedFrom befree-20150227 NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_assertion wasGeneratedBy ECO_0000203 NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP925097.RAUnrEBOtJ3lzsN_M8lebQw1BbeS_ZIJNzGw0ZfcNLiDA130_provenance.