Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_assertion description "[The aim of this study was to determine how often hematuria in families with TBMD segregated with haplotypes at the chromosomal loci for autosomal recessive and X-linked Alport syndrome (COL4A3/COL4A4 and COL4A5, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_assertion evidence source_evidence_literature NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_assertion SIO_000772 11318937 NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_assertion wasDerivedFrom befree-20150227 NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_assertion wasGeneratedBy ECO_0000203 NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320134.RA9N2-xpS8rPH2NlvYFL3nmmc5xMesPGqm-lopKV-tUFs130_provenance.