Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_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." NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_assertion evidence source_evidence_literature NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_assertion SIO_000772 15949572 NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_assertion wasDerivedFrom befree-20150227 NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_assertion wasGeneratedBy ECO_0000203 NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP925631.RAv6PI6_Wc78k0tGcBHXA4YwZ2kRRcAUnIRXtQ9pYM6Xc130_provenance.