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- source_evidence_literature type ECO_0000212 NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_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." NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_assertion evidence source_evidence_literature NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_assertion SIO_000772 19506355 NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_assertion wasDerivedFrom befree-2016 NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_assertion wasGeneratedBy ECO_0000203 NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.
- befree-2016 importedOn "2016-02-19" NP743872.RAgToAgAw8W1jBosPrEietHtdI2SzQT_D7TCR-ZU1WeLs130_provenance.