Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_assertion description "[A novel splice-site mutation in the CDH3 gene in hypotrichosis with juvenile macular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_assertion evidence source_evidence_literature NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_assertion SIO_000772 19076794 NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_assertion wasDerivedFrom befree-2016 NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_assertion wasGeneratedBy ECO_0000203 NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.
- befree-2016 importedOn "2016-02-19" NP708919.RAQNHLWgnOTGtR87taHsxbESH4ywZ-hLzkzR9zB9SbZDI130_provenance.