Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_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." NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_assertion evidence source_evidence_literature NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_assertion SIO_000772 19155175 NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_assertion wasDerivedFrom befree-20140225 NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_assertion wasGeneratedBy ECO_0000203 NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP725509.RAo-F3TiXfmN12iKZjtCR27lO2wLM22XhcjcVCMa3yVIw130_provenance.