Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_assertion description "[All together, our results indicate that mutations in IL1RAPL1 cause a spectrum of neurological impairments ranging from MR to high functioning autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_assertion evidence source_evidence_literature NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_assertion SIO_000772 18801879 NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_assertion wasDerivedFrom befree-2016 NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_assertion wasGeneratedBy ECO_0000203 NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.
- befree-2016 importedOn "2016-02-19" NP693868.RABu04HZi5AR-m0uk_05NLcuKoPgnRjnWgYxt0Zr-KBDo130_provenance.