Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_assertion> ?p ?o ?g. }
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- NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_assertion type Assertion NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_head.
- NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_assertion description "[Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_provenance.
- NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_assertion evidence source_evidence_literature NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_provenance.
- NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_assertion SIO_000772 19279310 NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_provenance.
- NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_assertion wasDerivedFrom befree-2016 NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_provenance.
- NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_assertion wasGeneratedBy ECO_0000203 NP725472.RAv4NCZFIbAYcZLIsGyeHnGS0cIM1_IkLEX7i8cahUdlw130_provenance.