Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_assertion wasGeneratedBy ECO_0000203 NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_assertion wasDerivedFrom befree-20150227 NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_assertion SIO_000772 16638984 NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_assertion evidence source_evidence_literature NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.
- NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_assertion description "[Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425730.RAtfdg1_NtM64Lxb8hMtah_Br8zIXWIwsF2D6KzkcD8QA130_provenance.