Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_assertion type Assertion NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_head.
- NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_assertion description "[FATP4 mutations in humans cause ichthyosis prematurity syndrome (IPS), and mutations of Fatp4 in mice have previously been found to cause a phenotype that resembles human congenital ichthyoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_provenance.
- NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_assertion evidence source_evidence_literature NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_provenance.
- NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_assertion SIO_000772 23226340 NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_provenance.
- NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_assertion wasDerivedFrom befree-20150227 NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_provenance.
- NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_assertion wasGeneratedBy ECO_0000203 NP858279.RAY7QAn5Hp5TsiFVBaEHczsA0twYBpInfYpqKShybpKQ0130_provenance.