Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_assertion evidence source_evidence_literature NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_assertion SIO_000772 16453125 NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_assertion wasDerivedFrom befree-20150227 NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_assertion wasGeneratedBy ECO_0000203 NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP328189.RARXSw6J9DgGV1E2Dj_tM8ROno9Kwm_UlLGr2K9cuVNYc130_provenance.