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- source_evidence_literature type ECO_0000212 NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_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." NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_assertion evidence source_evidence_literature NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_assertion SIO_000772 15821733 NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_assertion wasDerivedFrom befree-20150227 NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_assertion wasGeneratedBy ECO_0000203 NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP976668.RA22rXeyf-XfH50ueNj-WNM_BZ0S1gpQC3LsruWyInD2Y130_provenance.