Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_assertion type Assertion NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_head.
- NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_provenance.
- NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_assertion evidence source_evidence_literature NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_provenance.
- NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_assertion SIO_000772 11257260 NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_provenance.
- NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_assertion wasDerivedFrom befree-2016 NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_provenance.
- NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_assertion wasGeneratedBy ECO_0000203 NP311445.RAcaQ5YZD_1HsKGtcFVWEl3qH5jdofqVmEzWYS8eUgu1k130_provenance.