Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_assertion description "[MAP phenotype is similar to the FAP phenotype because of the somatic mutations to the APC gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_assertion evidence source_evidence_literature NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_assertion SIO_000772 21505584 NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_assertion wasDerivedFrom befree-20140225 NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_assertion wasGeneratedBy ECO_0000203 NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP807836.RAW7TULhhtqFopM47VlXLoKq0LOmZLqglSSpXh4VyZVyU130_provenance.