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- source_evidence_literature type ECO_0000212 NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_assertion description "[We describe the first mutation in SMAD8 in a patient with IPAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_assertion evidence source_evidence_literature NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_assertion SIO_000772 19211612 NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_assertion wasDerivedFrom gad-20150221 NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_assertion wasGeneratedBy ECO_0000203 NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP93839.RA61VNQrO0bWjzd1FfOsNL7_XdOQsYCSkZZPPW71xxfzE130_provenance.