Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_assertion description "[X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_assertion evidence source_evidence_literature NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_assertion SIO_000772 12177367 NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_assertion wasDerivedFrom befree-20140225 NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_assertion wasGeneratedBy ECO_0000203 NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP743393.RA3QRIcI1QMJX-OhlEgXAdgtsWEzW7o8qbmrG2BEDy4sI130_provenance.