Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_assertion evidence source_evidence_literature NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_assertion SIO_000772 11595972 NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_assertion wasDerivedFrom befree-20150227 NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_assertion wasGeneratedBy ECO_0000203 NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831134.RAwPZev5oQSeR7pv-u6UYiG58DBhg72iLOw-Yote-GfEo130_provenance.