Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_assertion description "[Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_assertion evidence source_evidence_literature NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_assertion SIO_000772 23219996 NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_assertion wasDerivedFrom befree-20140225 NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_assertion wasGeneratedBy ECO_0000203 NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP840337.RAWuFhRyVnX46UWpbMv4i3D1efHxTCANgFOybNJQHliC8130_provenance.