Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_assertion description "[We previously mapped a Seckel syndrome locus to chromosome 18p11.31-q11.2 (SCKL2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_assertion evidence source_evidence_literature NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_assertion SIO_000772 21998596 NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_assertion wasDerivedFrom befree-2016 NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_assertion wasGeneratedBy ECO_0000203 NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.
- befree-2016 importedOn "2016-02-19" NP931086.RAX2jqVvKoBOsfr-c9bKLJk8tac1KdBCHLSTrF7ExC7u0130_provenance.