Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion type Assertion NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_head.
- NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion wasGeneratedBy ECO_0000203 NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_provenance.
- NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion wasDerivedFrom befree-2016 NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_provenance.
- NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion SIO_000772 9684781 NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_provenance.
- NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion evidence source_evidence_literature NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_provenance.
- NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_assertion description "[The majority of patients with type 2N von Willebrand disease (VWD type 2N) have mutations in the region of the von Willebrand factor (VWF) gene encoding the factor VIII binding domain of VWF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1400782.RAcll4J4-e6uiZtyIz5z4WRRQrqtAugkZOGXQ3kdK13Cc130_provenance.