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- source_evidence_literature type ECO_0000212 NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_assertion description "[Although the aetiology of Williams syndrome (WS) is related to elastin gene disruption, its pathogenesis remains unknown, particularly that of vascular lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_assertion evidence source_evidence_literature NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_assertion SIO_000772 12095400 NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_assertion wasDerivedFrom befree-2016 NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_assertion wasGeneratedBy ECO_0000203 NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.
- befree-2016 importedOn "2016-02-19" NP359421.RA_WlalC-FsCk63eqyAjh7JNMdkknHkGH2ArEPPoUENJU130_provenance.