Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_assertion> ?p ?o ?g. }
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- NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_assertion type Assertion NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_head.
- NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_assertion wasGeneratedBy ECO_0000203 NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_provenance.
- NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_assertion wasDerivedFrom befree-20140225 NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_provenance.
- NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_assertion SIO_000772 15257456 NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_provenance.
- NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_assertion evidence source_evidence_literature NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_provenance.
- NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_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." NP334775.RAexk1hmWsfxXGwd6NugQoAPW_J5idl-ICQ_caOhj1cB0130_provenance.