Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_assertion description "[We report chromosomal localization of INT2/HST1 amplification in OSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_assertion evidence source_evidence_literature NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_assertion SIO_000772 7539284 NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_assertion wasDerivedFrom befree-20140225 NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_assertion wasGeneratedBy ECO_0000203 NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP521387.RAaD0Nbnp1rsWJrxkpYLNaDFV8AkEXNKfTnIBSIgvLsjc130_provenance.