Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_assertion description "[A cohort of 84 familial congenital or juvenile cataract index cases was screened for mutations in the EPHA2 gene by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_assertion evidence source_evidence_literature NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_assertion SIO_000772 24014202 NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_assertion wasDerivedFrom befree-20150227 NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_assertion wasGeneratedBy ECO_0000203 NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP371723.RAikRZ7A2oE7DbkENfaKUJKDsRbdAhd4tczY0Q2roR6Bo130_provenance.