Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_assertion description "[Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_assertion evidence source_evidence_literature NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_assertion SIO_000772 21109226 NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_assertion wasDerivedFrom befree-20140225 NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_assertion wasGeneratedBy ECO_0000203 NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP296112.RAw8_6LeNK5NA1E6gSs4Hf351dw-NGBSZEpmALtHx5WS4130_provenance.