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- source_evidence_literature type ECO_0000212 NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_assertion description "[The most frequently mutated genes specify proteins implicated in chromatin remodeling: 44% of the tumors had somatic inactivating mutations in MEN1, which encodes menin, a component of a histone methyltransferase complex, and 43% had mutations in genes encoding either of the two subunits of a transcription/chromatin remodeling complex consisting of DAXX (death-domain-associated protein) and ATRX (? thalassemia/mental retardation syndrome X-linked).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_assertion evidence source_evidence_literature NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_assertion SIO_000772 21252315 NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_assertion wasDerivedFrom befree-20150227 NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_assertion wasGeneratedBy ECO_0000203 NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP347491.RAVUU_xlv-mTEctssKjLNoHdmt8a-2f8y0sMzLoZkB0Sg130_provenance.