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- NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_assertion type Assertion NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_head.
- NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_assertion description "[The histological pattern suggestive of CNM in the fetuses can expand the spectrum of genes causing CNM, as we propose that mutations in ECEL1 can cause CNM or a condition similar to this.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_provenance.
- NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_assertion evidence source_evidence_literature NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_provenance.
- NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_assertion SIO_000772 25708584 NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_provenance.
- NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_assertion wasDerivedFrom befree-2016 NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_provenance.
- NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_assertion wasGeneratedBy ECO_0000203 NP1265852.RAQTWCjXxnio0cL0XDEXZnG5Bk0d_cj6QnCiU932gVLXo130_provenance.