Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_assertion description "[Twenty-one unrelated children with persistent familial hematuria as well as their families were studied for segregation of hematuria with haplotypes at the COL4A3/COL4A4 locus for benign familial hematuria and at the COL4A5 locus for X-linked Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_assertion evidence source_evidence_literature NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_assertion SIO_000772 16235097 NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_assertion wasDerivedFrom befree-20150227 NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_assertion wasGeneratedBy ECO_0000203 NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP319940.RAijiG_kiTHsf--8hSqoWQh4tYOnHk_ln7C-sg9hKmLuE130_provenance.