Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion wasGeneratedBy ECO_0000203 NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion wasDerivedFrom befree-20140225 NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion SIO_000772 21236492 NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion evidence source_evidence_literature NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP536688.RA7RixuGVCz16FRjpPwHiNFbj5aV6fZTK26cnGBVS0sx8130_provenance.