Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_assertion description "[In humans, mutations in TMEM67 (also known as MKS3) cause both MKS and JBTS, with TMEM67 encoding the orphan receptor meckelin (TMEM67) that localizes to the ciliary transition zone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_assertion evidence source_evidence_literature NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_assertion SIO_000772 23283079 NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_assertion wasDerivedFrom befree-2016 NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_assertion wasGeneratedBy ECO_0000203 NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1040157.RA2uOgfz5UGTsiSU6FTrhL7ruINTerqePUaFqU2klR6zI130_provenance.