Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_assertion description "[To our knowledge, this is the first report of successful simultaneous detection of multiple genetic polymorphisms with point mutations using ASPCR-MP or multiple genetic polymorphisms with large structural alterations using stepdown PCR. In conclusion, AS]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_assertion evidence source_evidence_literature NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_assertion SIO_000772 15691505 NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_assertion wasDerivedFrom gad-20150221 NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_assertion wasGeneratedBy ECO_0000203 NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.
- gad-20150221 importedOn "2015-02-21" NP90450.RAPViFotT_iWq8nX5LH8_lADwMEQPj-UQaox9tiVap-0Q130_provenance.