Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_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." NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_assertion evidence source_evidence_literature NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_assertion SIO_000772 19506355 NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_assertion wasDerivedFrom befree-20140225 NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_assertion wasGeneratedBy ECO_0000203 NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP158087.RAKDCmeRErOf_AMad3sn6Jnnh5FPmJlRSWV49gkLiyiRo130_provenance.