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- source_evidence_literature type ECO_0000212 NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_assertion evidence source_evidence_literature NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_assertion SIO_000772 17221017 NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_assertion wasDerivedFrom befree-20150227 NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_assertion wasGeneratedBy ECO_0000203 NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978198.RAkTPbbt2XJ2o2hPgn_EzoGDuhRJ5bUT3DV3jnrOtASck130_provenance.