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- source_evidence_literature type ECO_0000212 NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_assertion description "[Seven novel DAX1 mutations with loss of function identified in Chinese patients with congenital adrenal hypoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_assertion evidence source_evidence_literature NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_assertion SIO_000772 20573681 NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_assertion wasDerivedFrom befree-2016 NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_assertion wasGeneratedBy ECO_0000203 NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.
- befree-2016 importedOn "2016-02-19" NP820973.RAKXci6Iujv-O5dY7l2p3_gf5C4nbWr__kYCkM3x2YVno130_provenance.