Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in a]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_assertion evidence source_evidence_literature NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_assertion SIO_000772 20591486 NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_assertion wasDerivedFrom gad-20150221 NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_assertion wasGeneratedBy ECO_0000203 NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP180187.RAU7tv6RAPbbVmaD5bIA1HI_eluCG2wm5Hg6NSppH_lsE130_provenance.