Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP643389.RAjiBUZcJ_cXZ9JTaEOjBMyMElDesmbn77Lv4CDX0Grac130_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." NP643389.RAjiBUZcJ_cXZ9JTaEOjBMyMElDesmbn77Lv4CDX0Grac130_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.
- NP283820.RAHW2e48dycoti9YZeomGji8sjOozM8zKmlnkeIIZ5aDo130_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." NP283820.RAHW2e48dycoti9YZeomGji8sjOozM8zKmlnkeIIZ5aDo130_provenance.