Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion description "[Escobar syndrome has been recently described as a prenatal form of myasthenia associated with recessive mutations in genes of the neuromuscular junction (CHRNG, CHRNA1, CHRND, RAPSN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion evidence source_evidence_literature NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion SIO_000772 19155175 NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion wasDerivedFrom befree-20150227 NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_assertion wasGeneratedBy ECO_0000203 NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP314607.RAfPN8yGFHOBjh34sHnOppIIF5xppr4IooBOapU1EG0VM130_provenance.