Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_assertion> ?p ?o ?g. }
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- NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_assertion type Assertion NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_head.
- NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_assertion wasGeneratedBy ECO_0000218 NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_provenance.
- NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_assertion wasDerivedFrom ctd_human-20130708 NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_provenance.
- NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_assertion SIO_000772 16845274 NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_provenance.
- NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_assertion evidence source_evidence_curated NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_provenance.
- NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_assertion description "[Although RAI1 is the primary gene responsible for most features of SMS, other genes within 17p11.2 contribute to the variable features and overall severity of the syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28132.RAW2Dp972VinD3vAi2wXnmpnZwup3KjaimG9VR4mgjmw8130_provenance.