Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_assertion description "[In conclusion, we found a significant association of INSL3 gene mutations in men presenting one or more signs of TDS syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_assertion evidence source_evidence_literature NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_assertion SIO_000772 16687567 NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_assertion wasDerivedFrom befree-20140225 NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_assertion wasGeneratedBy ECO_0000203 NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP730278.RAiNfW1lTBoe2fcRIL3J_Lb9l5hTH-KVOUljfVXIct4Rk130_provenance.