Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_assertion description "[Independent risk factors for syncope in genotype-negative subjects included female sex (hazard ratio [HR], 1.60; P=0.002), prolonged QTc (HR=1.63 per 100 ms increment, P=0.02), family history of ACA or SCD (HR=1.89, P=0.002), and LQT2 versus LQT1 family mutation (HR=1.41, P=0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_assertion evidence source_evidence_literature NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_assertion SIO_000772 21831960 NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_assertion wasDerivedFrom befree-20150227 NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_assertion wasGeneratedBy ECO_0000203 NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP701950.RANqQRbQTHmW5ldHm3f89MwRyRaqgESsrgWD8U-p7xvrs130_provenance.