Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_assertion> ?p ?o ?g. }
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- NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_assertion type Assertion NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_head.
- NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_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." NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_provenance.
- NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_assertion evidence source_evidence_literature NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_provenance.
- NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_assertion SIO_000772 23226340 NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_provenance.
- NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_assertion wasDerivedFrom befree-2016 NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_provenance.
- NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_assertion wasGeneratedBy ECO_0000203 NP1034861.RA5Tin2wACcfME6RQHMVzlsvIanUBwotPAt_SgObBBD2s130_provenance.