Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_assertion description "[CDKN2 does not appear to be the only TSG on 9p21 in HNSCC, and our results suggest that another region of deletion exists proximal to the IFNW locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_assertion evidence source_evidence_literature NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_assertion SIO_000772 7542912 NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_assertion wasDerivedFrom befree-20140225 NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_assertion wasGeneratedBy ECO_0000203 NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP237931.RAPWaCwJ8EMG2XUranN3N5BV1EB0NeJz8dCewPj0gL7Hc130_provenance.