Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_assertion description "[The authors analyzed microsatellites on chromosome 17q 21.3-22 (nm23), 3p 25-26 (von Hippel Lindau disease [VHL] gene), and 5q 21-22 (D5S346 locus) in 12 synchronous ovarian and appendiceal mucinous lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_assertion evidence source_evidence_literature NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_assertion SIO_000772 8617458 NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_assertion wasDerivedFrom befree-2016 NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_assertion wasGeneratedBy ECO_0000203 NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1348518.RAy_sj6_HF67ON7xBBG6d8uLYUqXbho2tq_fdi7sqbsQs130_provenance.