Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_assertion description "[These results show that the APAF1 variants associated with risk for MDD in the Utah pedigrees are very rare in Northern European and European-American populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_assertion evidence source_evidence_literature NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_assertion SIO_000772 19455599 NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_assertion wasDerivedFrom befree-20150227 NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_assertion wasGeneratedBy ECO_0000203 NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.
- befree-20150227 importedOn "2015-02-27" NP240228.RAPjLFZL2r5Iz9wTbvkF0JEFkjzuAlySIWGt0IB8OBtck130_provenance.