Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_assertion type Assertion NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_head.
- NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_assertion description "[A mutation in the B-box region of TRIM32 has also been shown to result in a more pleiotropic disorder, Bardet-Biedl Syndrome (BBS11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_provenance.
- NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_assertion evidence source_evidence_literature NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_provenance.
- NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_assertion SIO_000772 21496629 NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_provenance.
- NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_assertion wasDerivedFrom befree-20150227 NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_provenance.
- NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_assertion wasGeneratedBy ECO_0000203 NP866674.RAhiU76fs8YG8mmMfGE1xhOtG0dQFj_GK_3vfLxb0ALmI130_provenance.