Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_assertion wasGeneratedBy ECO_0000203 NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_assertion wasDerivedFrom befree-20150227 NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_assertion SIO_000772 21114141 NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_assertion evidence source_evidence_literature NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.
- NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_assertion description "[A novel de novo SCN1A missense mutation in Severe Myoclonic Epilepsy Borderland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682408.RADB45g74CiY7WTaQji4kMYhGDz0Yq8ZFhK6LaSExqYL4130_provenance.