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- source_evidence_literature type ECO_0000212 NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion description "[The defective FVIII carrier function of von Willebrand factor (VWF) identifies type 2N von Willebrand disease (VWD), a variant with a pattern resembling hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion evidence source_evidence_literature NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion SIO_000772 17456630 NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion wasDerivedFrom befree-2016 NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_assertion wasGeneratedBy ECO_0000203 NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.
- befree-2016 importedOn "2016-02-19" NP606311.RAfvUlDuhH3Dzsvq-XhpxfvNiLz5uNAVlnSw-yG5IOib0130_provenance.