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- NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_assertion type Assertion NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_head.
- NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_assertion description "[Within a series of BRCA1 and BRCA2 mutation-negative families, a germline TP53 13398 G>A (Arg213Gln) mutation was identified, which was selected for mutation analysis in this gene because of a family history consistent with Li-Fraumeni syndrome (LFS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_provenance.
- NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_assertion evidence source_evidence_literature NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_provenance.
- NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_assertion SIO_000772 17541742 NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_provenance.
- NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_assertion wasDerivedFrom befree-20140225 NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_provenance.
- NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_assertion wasGeneratedBy ECO_0000203 NP802066.RANLaMD96Z612clpbNLNCRHBkMRRP8ROVTZ5aRHr9Jtto130_provenance.