Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_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." NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_assertion evidence source_evidence_literature NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_assertion SIO_000772 11595972 NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_assertion wasDerivedFrom befree-20140225 NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_assertion wasGeneratedBy ECO_0000203 NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP663743.RARKvxGDiza8omT-hQDPYNaFY3h-H4nqaeEgfypurXxVM130_provenance.