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- source_evidence_literature type ECO_0000212 NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_assertion description "[We examined our patient population with episodic ataxia and hemiplegic migraine but with no mutation in either CACNA1A or ATP1A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_assertion evidence source_evidence_literature NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_assertion SIO_000772 16116111 NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_assertion wasDerivedFrom befree-2016 NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_assertion wasGeneratedBy ECO_0000203 NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.
- befree-2016 importedOn "2016-02-19" NP510179.RAe-yy8Oy6jtXzd6eogQ_T2aLJ7FAEcv2fGhMAI2fX-54130_provenance.