Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_assertion description "[Platelet-type von Willebrand disease (PT-VWD) is a rare bleeding disorder that results from gain-of-function mutations in the GPIBA gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_assertion evidence source_evidence_literature NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_assertion SIO_000772 15705799 NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_assertion wasDerivedFrom befree-20140225 NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_assertion wasGeneratedBy ECO_0000203 NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722412.RA2eXWWeNqolG4qkCdrIOx7qSbwbTXXqLJxNahvkPyI68130_provenance.