Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion type Assertion NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_head.
- NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion description "[Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_provenance.
- NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion evidence source_evidence_literature NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_provenance.
- NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion SIO_000772 19221116 NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_provenance.
- NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion wasDerivedFrom gad-20130706 NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_provenance.
- NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_assertion wasGeneratedBy ECO_0000203 NP79550.RAgtLPEvaN7Zf7sx9u5A9Bl8DQqIZNaNv3re2yyjpr9DI130_provenance.