Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_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." NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion evidence source_evidence_literature NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion SIO_000772 25182519 NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion wasDerivedFrom befree-20150227 NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_assertion wasGeneratedBy ECO_0000203 NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP954021.RAoxaV0l6ZUeFgJ3N0IzUFpmMIaPTuq1f0-RDvFrlHt8M130_provenance.