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- source_evidence_literature type ECO_0000212 NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_assertion description "[We identified mutations in a new human gene, ESCO2, associated with Roberts syndrome in 15 kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_assertion evidence source_evidence_literature NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_assertion SIO_000772 15821733 NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_assertion wasDerivedFrom befree-2016 NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_assertion wasGeneratedBy ECO_0000203 NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.
- befree-2016 importedOn "2016-02-19" NP489327.RAMQ4gpXnmsS45IMT9tnSFNjly1SxiyHRneasI_3ccgY0130_provenance.