Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_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." NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_assertion evidence source_evidence_literature NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_assertion SIO_000772 19161143 NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_assertion wasDerivedFrom befree-20140225 NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_assertion wasGeneratedBy ECO_0000203 NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615687.RAkncP4IbQwzUrE0B-1te97xciGvgOm2uUGbVDI34F8_I130_provenance.