Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_assertion> ?p ?o ?g. }
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- NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_assertion type Assertion NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_head.
- NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_assertion wasGeneratedBy ECO_0000203 NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_provenance.
- NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_assertion wasDerivedFrom befree-2016 NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_provenance.
- NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_assertion SIO_000772 15257456 NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_provenance.
- NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_assertion evidence source_evidence_literature NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_provenance.
- NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_assertion description "[It has been previously shown that mutations in a particular nucleotide in CHX10 are associated with an autosomal recessive syndrome of microphthalmia/anophthalmia with iris colobomas and cataracts in two families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP452292.RAPBE4_xvybxSeux7MPKBwr3jDCE5C-P-SZy9dcoLtcRg130_provenance.