Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_assertion description "[However, the absence of MSX2 mutations in some of the FPP patients analysed and the presence of FPP associated with chromosome 11p deletions in DEFECT 11 (OMIM 601224) patients or associated with Saethre-Chotzen syndrome suggests genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_assertion evidence source_evidence_literature NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_assertion SIO_000772 11106354 NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_assertion wasDerivedFrom befree-20150227 NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_assertion wasGeneratedBy ECO_0000203 NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP571789.RAwViNyDsxIp1MGDqJX8kCw-SUR_pW0RFFWvz6TNGZpsI130_provenance.