Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_assertion description "[We have systematically compared RNASEQR with four of the most widely used tools using a simulated data set created from the Consensus CDS project and two experimental RNA-seq data sets generated from a human glioblastoma patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_assertion evidence source_evidence_literature NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_assertion SIO_000772 22199257 NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_assertion wasDerivedFrom befree-2016 NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_assertion wasGeneratedBy ECO_0000203 NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.
- befree-2016 importedOn "2016-02-19" NP949288.RANMBlcHZ1m8J2UayOigMMFrp915cgOQ6kC8QMc0Xw2Mc130_provenance.