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- source_evidence_literature type ECO_0000212 NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_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." NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_assertion evidence source_evidence_literature NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_assertion SIO_000772 19506355 NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_assertion wasDerivedFrom befree-20150227 NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_assertion wasGeneratedBy ECO_0000203 NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392325.RAy-sLEBo3vkANh6hQZz5orfOxRo-V3mLE8sBKH20D5iw130_provenance.