Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_assertion description "[Although TBMN is an autosomal dominant disease (COL4A3 and COL4A4), ATS can be inherited X-linked (COL4A5), autosomal recessive, or autosomal dominant (both COL4A3 and COL4A4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_assertion evidence source_evidence_literature NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_assertion SIO_000772 20177710 NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_assertion wasDerivedFrom befree-20140225 NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_assertion wasGeneratedBy ECO_0000203 NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP213071.RA2aptwGwQP67c0cNiJVcl4_RT-dUtqzTc8a3kSfVZkCM130_provenance.