Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_assertion description "[Recently, we identified a frameshift mutation in the CDH3 gene encoding P-cadherin as the proximal cause of hypotrichosis with juvenile macular dystrophy in four families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_assertion evidence source_evidence_literature NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_assertion SIO_000772 12445216 NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_assertion wasDerivedFrom befree-20140225 NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_assertion wasGeneratedBy ECO_0000203 NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP268147.RAoEu0UG8oNG4Mc74iqwqgLwVKz7flX0pKlVkp3YvCUfs130_provenance.