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- source_evidence_literature type ECO_0000212 NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_assertion description "[Mutations in the Aristaless-related homeobox (ARX) gene are associated with pleiotropic phenotypes including infantile spasms, mental retardation and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_assertion evidence source_evidence_literature NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_assertion SIO_000772 18823727 NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_assertion wasDerivedFrom befree-20140225 NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_assertion wasGeneratedBy ECO_0000203 NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP249210.RAogU-L5vt0siX_jWWCwyNlsfoJ1gFriuVb9puinwW5dw130_provenance.