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- NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_assertion type Assertion NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_head.
- NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_assertion description "[This concise review is focused on genetic, molecular and clinical aspects of von Willebrand disease (VWD) type 2N and of mild hemophilia A due to mutations impairing FVIII-von Willebrand factor (VWF) interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_provenance.
- NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_assertion evidence source_evidence_literature NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_provenance.
- NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_assertion SIO_000772 19506355 NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_provenance.
- NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_assertion wasDerivedFrom befree-2016 NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_provenance.
- NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_assertion wasGeneratedBy ECO_0000203 NP743877.RAG1Vdsw6HDMJ1TPb-JeL_ajLla61MnN94f4LEHGHlI_U130_provenance.