Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_assertion description "[Two of the affected males demonstrated a severe form of choroideremia with low or nondetectable ERG recordings, while the other two affected males showed a less severe phenotype with only a slight reduction of the ERG amplitudes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_assertion evidence source_evidence_literature NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_assertion SIO_000772 8749050 NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_assertion wasDerivedFrom befree-20150227 NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_assertion wasGeneratedBy ECO_0000203 NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP382990.RA_C28W_P780XnJNTEO_BXH2rKK-ZGjhnsbeIest_1sQU130_provenance.