Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_assertion description "[We herein report a patient with a concurrent deletion of BMP4 and OTX2 who exhibited bilateral microphthalmia, more specifically, anterior segment dysgenesis with microcornea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_assertion evidence source_evidence_literature NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_assertion SIO_000772 23103883 NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_assertion wasDerivedFrom befree-2016 NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_assertion wasGeneratedBy ECO_0000203 NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.
- befree-2016 importedOn "2016-02-19" NP1024281.RAeleRUelGwNKxx6Ma9Og_x0hAgJmIjREvILBrHHnjC2U130_provenance.