Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_assertion description "[The role of p16(INK4A)/p14(ARF) and p53 mutations in sporadic glioma provides a strong rationale for investigating germline mutations in these genes as a cause of familial glioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_assertion evidence source_evidence_literature NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_assertion SIO_000772 20455025 NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_assertion wasDerivedFrom befree-20140225 NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_assertion wasGeneratedBy ECO_0000203 NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785633.RArZVWxpBrcZRl767b-xBHwXMlrBw69MwgzYINfnM4dLU130_provenance.