Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_assertion description "[In addition, sequencing of the B3GALTL gene, the gene implicated in Peters-plus syndrome did not reveal any mutation in the sibs reported here.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_assertion evidence source_evidence_literature NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_assertion SIO_000772 19161143 NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_assertion wasDerivedFrom befree-20150227 NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_assertion wasGeneratedBy ECO_0000203 NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974147.RAKhX4pzxv86iVnGVBKmTQhCkpW5CQZyCnefGqLsa-zZk130_provenance.