Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion description "[One novel deletion and one splicing mutation of the LKB1 gene in two Chinese patients with Peutz-Jeghers syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion evidence source_evidence_literature NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion SIO_000772 22928647 NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion wasDerivedFrom befree-2016 NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_assertion wasGeneratedBy ECO_0000203 NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1008661.RAhXk8BDL2VHaIvV_DmTnh2_wzmQoRlxJBldOAPCKBJ0E130_provenance.