Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_assertion type Assertion NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_head.
- NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_assertion wasGeneratedBy ECO_0000203 NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_provenance.
- NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_assertion wasDerivedFrom befree-20140225 NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_provenance.
- NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_assertion SIO_000772 15930903 NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_provenance.
- NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_assertion evidence source_evidence_literature NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_provenance.
- NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_assertion description "[The only other similar case with a deletion of 20p11.22-p11.23 exhibited a phenotype that also included abnormal neural development (autism, craniofacial dysmorphism, and Hirschsprung disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP330312.RAq84l4rJY0urgGii4gN3NFb7rE8HF-W2d7trlFiwWbjY130_provenance.