Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion type Assertion NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_head.
- NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion description "[Missense mutations in the FVIII gene impairing the binding to VWF are a common cause of mild/moderate hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_provenance.
- NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion evidence source_evidence_literature NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_provenance.
- NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion SIO_000772 19506355 NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_provenance.
- NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion wasDerivedFrom befree-2016 NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_provenance.
- NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_assertion wasGeneratedBy ECO_0000203 NP743873.RAlPerk17Zpr4PR8Bth_pN6l_lRn1GkfWO_1DtD6QA3vI130_provenance.