Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_assertion description "[A GP1BB missense mutation suppresses GPIb/IX complex expression and is found to cause Bernard-Soulier Syndrome in the homozygous form and giant platelets in the heterozygous form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_assertion evidence source_evidence_literature NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_assertion SIO_000772 11816714 NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_assertion wasDerivedFrom lhgdn-20090331 NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_assertion wasGeneratedBy ECO_0000203 NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193080.RAfuR89p9r1oEIMtIWr0AIK3NXvfeojBhHF53SY-k_J_0130_provenance.