Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_assertion> ?p ?o ?g. }
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- NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_assertion type Assertion NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_head.
- NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_assertion description "[While non-malformation phenotypes tend to be caused by pathogenic variations that are predicted to expand the first two polyalanine tracts of ARX, or alter residues outside of the homeodomain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_provenance.
- NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_assertion evidence source_evidence_literature NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_provenance.
- NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_assertion SIO_000772 19507262 NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_provenance.
- NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_assertion wasDerivedFrom befree-2016 NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_provenance.
- NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_assertion wasGeneratedBy ECO_0000203 NP744033.RAq0pR-SH0il8L0rBoAKOI8CWuYZK1sC18ffrZ21Rvf1c130_provenance.