Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_assertion> ?p ?o ?g. }
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- NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_assertion type Assertion NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_head.
- NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_assertion wasGeneratedBy ECO_0000203 NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_provenance.
- NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_assertion wasDerivedFrom befree-20150227 NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_provenance.
- NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_assertion SIO_000772 20967465 NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_provenance.
- NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_assertion evidence source_evidence_literature NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_provenance.
- NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_assertion description "[Rather, our findings suggest that loss-of-function mutations of RAB3GAP1 as well as functionally severe RAB3GAP2 mutations cause Warburg Micro syndrome while hypomorphic RAB3GAP2 mutations can result in the milder Martsolf phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866053.RA-_mtlku9XpNiZ_w4YSwQzBT5f_8EnZS5J75Aw3Czbnw130_provenance.