Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_assertion description "[Collectively, identification of mutations in the MRP6 gene provides the basis to examine the pathomechanisms of PXE and allows development of DNA-based carrier detection, prenatal testing, and preimplantation genetic diagnosis in families with a history of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_assertion evidence source_evidence_literature NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_assertion SIO_000772 10811882 NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_assertion wasDerivedFrom befree-2016 NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_assertion wasGeneratedBy ECO_0000203 NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.
- befree-2016 importedOn "2016-02-19" NP283959.RAEnDULDkedNyoapVN0VzeeXVNqRbFGtl4www2i1boi04130_provenance.