Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_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." NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_assertion evidence source_evidence_curated NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_assertion SIO_000772 19068278 NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_assertion wasDerivedFrom ctd_human-20130708 NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_assertion wasGeneratedBy ECO_0000218 NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP31371.RATckAHlD7AEeJS8WL6cb9B6klj_hqRmbISq_hJJsXACY130_provenance.