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- NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_assertion type Assertion NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_head.
- NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_assertion description "[The disease is frequently caused by intron 22 inversion mutation in FVIII gene in approximately 50% cases and by intron 1 inversion (Inv1) in 2% to 5% cases with severe hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_provenance.
- NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_assertion evidence source_evidence_literature NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_provenance.
- NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_assertion SIO_000772 22371627 NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_provenance.
- NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_assertion wasDerivedFrom befree-20150227 NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_provenance.
- NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_assertion wasGeneratedBy ECO_0000203 NP392307.RAZMxfrOUzcHvbTa4cAB0qQZlt0AyW174LA_RuM0cE6z0130_provenance.