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- NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_assertion type Assertion NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_head.
- NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_assertion description "[Within our cohort, we confirm the association of PTEN mutations and extreme macrocephaly (>3 SD, 99.7th percentile) and identify mutations in 22% of cases, including three novel PTEN mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_provenance.
- NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_assertion evidence source_evidence_literature NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_provenance.
- NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_assertion SIO_000772 23361946 NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_provenance.
- NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_assertion wasDerivedFrom befree-2016 NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_provenance.
- NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_assertion wasGeneratedBy ECO_0000203 NP1048372.RATRWAb5redugRM6xaeE-DrD2vnaCTdouia1FuX_mRSQ0130_provenance.