Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_assertion description "[We report five new genes associated with this condition and suggest screening of TFAP2A and FLNA in patients with Peters anomaly and relevant syndromic features and HCCS, NDP and SLC4A11 in patients with isolated Peters anomaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_assertion evidence source_evidence_literature NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_assertion SIO_000772 25182519 NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_assertion wasDerivedFrom befree-2016 NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_assertion wasGeneratedBy ECO_0000203 NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP1216281.RAwXIlD-EVLoK3MKP8m-VtPg4JNSgaOfN7jEos692v_3Y130_provenance.