Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_assertion wasGeneratedBy ECO_0000203 NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_assertion wasDerivedFrom befree-20140225 NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_assertion SIO_000772 17236141 NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_assertion evidence source_evidence_literature NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_assertion description "[Our data established the link between HOXD13 and two additional limb phenotypes--syndactyly type V and brachydactyly type A4--and demonstrated that a polyalanine contraction in HOXD13, most likely, led to other digital anomalies but not to synpolydactyly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP821023.RALkexz6UoitMNu_uYcx63CG4UeeJGVtDsnBQjmwKboBI130_provenance.