Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_assertion description "[TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_assertion evidence source_evidence_curated NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_assertion SIO_000772 19068278 NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_assertion wasDerivedFrom ctd_human-2016 NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_assertion wasGeneratedBy ECO_0000218 NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP23086.RAsmD1ETkgapUxvqQzAAkyHMl_jljGHBrStC54_HFGJcs130_provenance.