Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_assertion description "[The effects of individual point mutations on the folding state and stability of the ADD domain correlate well with the levels of mutant ATRX protein in patients, providing insights into the molecular pathophysiology of ATR-X syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_assertion evidence source_evidence_literature NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_assertion SIO_000772 17609377 NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_assertion wasDerivedFrom befree-2016 NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_assertion wasGeneratedBy ECO_0000203 NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.
- befree-2016 importedOn "2016-02-19" NP618353.RAWW5fhsVg9dfTCSukbxU1YYhharlGJwgJ9D7ns6qG_Yc130_provenance.