Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_assertion description "[We previously mapped a Seckel syndrome locus to chromosome 18p11.31-q11.2 (SCKL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_assertion evidence source_evidence_literature NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_assertion SIO_000772 21998596 NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_assertion wasDerivedFrom befree-20140225 NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_assertion wasGeneratedBy ECO_0000203 NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925313.RAQ2gU_WO9BVfQ8ANZ62E6792qNtU-3h5ruXchYPO-CrY130_provenance.