Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_assertion description "[To identify mutations in the TGFBI gene in Indian patients with lattice corneal dystrophy (LCD) or granular corneal dystrophy (GCD) and to look for genotype-phenotype correlations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_assertion evidence source_evidence_literature NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_assertion SIO_000772 15623763 NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_assertion wasDerivedFrom befree-2016 NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_assertion wasGeneratedBy ECO_0000203 NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.
- befree-2016 importedOn "2016-02-19" NP474482.RAT77_1vhcif6DBvQo3Qno84DIxiZ3Yb8uRGVltySKyUg130_provenance.