Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_assertion description "[Patients with two SLC3A1 mutations are classified as type A cystinuria, whereas patients with two SLC7A9 mutations are classified as type B cystinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_assertion evidence source_evidence_literature NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_assertion SIO_000772 16374432 NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_assertion wasDerivedFrom befree-2016 NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_assertion wasGeneratedBy ECO_0000203 NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.
- befree-2016 importedOn "2016-02-19" NP528273.RA7h60Uv3IJGjgpvtvNf2gdYp8VeLXujDPM5yH64NZ7_I130_provenance.