Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_assertion> ?p ?o ?g. }
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- NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_assertion type Assertion NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_head.
- NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_assertion description "[genetic variation in the ALOX5AP gene contributes to CHD risk in patients with FH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_provenance.
- NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_assertion evidence source_evidence_literature NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_provenance.
- NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_assertion SIO_000772 18775537 NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_provenance.
- NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_assertion wasDerivedFrom gad-20150221 NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_provenance.
- NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_assertion wasGeneratedBy ECO_0000203 NP129610.RAl_sbkFX6YQX3NChZVFAj6-ray6UO47eHODF22CA5yGs130_provenance.