Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_assertion wasGeneratedBy ECO_0000203 NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_assertion wasDerivedFrom gad-20150221 NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_assertion SIO_000772 19336355 NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_assertion evidence source_evidence_literature NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.
- NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_assertion description "[We performed genotypic analysis for factor V G1691A, factor II G20210A, methylenetetrahydrofolate reductase C677T, and 4 common platelet glycoprotein polymorphisms (human platelet alloantigen-1, -2, -3, and -5) in 150 children <18 years of age with established diagnoses of stroke, transient ischemic attack, or migraine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79504.RAq0Ket7AVk-9UN2BW8igvJub6hr4RtqZ7ljx6L8KIXHA130_provenance.