Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_assertion description "[Naturally occurring CaR mutations with differences in dominant-negative effect on wild-type receptor demonstrate differences in biochemical severity in FHH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_assertion evidence source_evidence_literature NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_assertion SIO_000772 16649980 NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_assertion wasDerivedFrom befree-20150227 NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_assertion wasGeneratedBy ECO_0000203 NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP692393.RAl4mdQSlFK6YTGVzORQWbhGwf7mc8GAS0D1G5Mwioucs130_provenance.