Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_assertion description "[Polymorphisms in PDE9A and PDE11A were found to be associated with the diagnosis of MDD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_assertion evidence source_evidence_literature NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_assertion SIO_000772 17008408 NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_assertion wasDerivedFrom befree-2016 NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_assertion wasGeneratedBy ECO_0000203 NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.
- befree-2016 importedOn "2016-02-19" NP571845.RAf1lBvLcNTwywuzpMaLDqzmCH23afgIghEieNN4sbYVo130_provenance.