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- source_evidence_literature type ECO_0000212 NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_assertion description "[Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_assertion evidence source_evidence_literature NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_assertion SIO_000772 20729831 NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_assertion wasDerivedFrom befree-2016 NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_assertion wasGeneratedBy ECO_0000203 NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.
- befree-2016 importedOn "2016-02-19" NP834349.RAdiro4YsKDnvoY2Dri6Q-i5zoi9F2aZZweCdpSxMTFDE130_provenance.