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- source_evidence_literature type ECO_0000212 NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_assertion wasGeneratedBy ECO_0000203 NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_assertion wasDerivedFrom befree-20140225 NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_assertion SIO_000772 19723756 NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_assertion evidence source_evidence_literature NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_assertion description "[The aim of the study was to identify the GATA3 mutation in a HDR patient and determine its functional consequences.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP200766.RA2voM70YjMHxO5B44njdvgixBOAK0riylH8d5BzQIqCU130_provenance.