Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_assertion description "[Mutations in LCA5 are a rare cause of childhood retinal dystrophy accounting for ?2% of disease in this cohort, and the majority of LCA5 mutations are likely null.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_assertion evidence source_evidence_literature NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_assertion SIO_000772 23946133 NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_assertion wasDerivedFrom befree-20150227 NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_assertion wasGeneratedBy ECO_0000203 NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977711.RA6DrdXk20O2p7GITbGmdxV_kXF3AEKQPqt17Ts0nxqi0130_provenance.