Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_assertion description "[Mutations in collagen type IV genes have been described to be responsible for X-linked (COL4A5), autosomal recessive, and autosomal dominant AS (COL4A3/COL4A4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_assertion evidence source_evidence_literature NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_assertion SIO_000772 14582039 NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_assertion wasDerivedFrom befree-20140225 NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_assertion wasGeneratedBy ECO_0000203 NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP414610.RAlgn6NL8G_UXZ7_-e6HfNeXl8fhSY8wvkTJomVXGnQoY130_provenance.