Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_assertion description "[Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_assertion evidence source_evidence_literature NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_assertion SIO_000772 8875187 NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_assertion wasDerivedFrom befree-20140225 NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_assertion wasGeneratedBy ECO_0000203 NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP890462.RAaK6Nsm2UFNH5G31q1UEHDcm55Id1NzL_KtxSiZ-1-CU130_provenance.