Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_assertion> ?p ?o ?g. }
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- NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_assertion type Assertion NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_head.
- NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_assertion description "[Among them, Sotos and Weaver syndromes are clinically well defined and due to heterozygous mutations in NSD1 and EZH2, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_provenance.
- NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_assertion evidence source_evidence_literature NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_provenance.
- NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_assertion SIO_000772 24852293 NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_provenance.
- NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_assertion wasDerivedFrom befree-2016 NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_provenance.
- NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_assertion wasGeneratedBy ECO_0000203 NP1184587.RAhg9pIlXbgzuNc6FU7Qv6JMxt1rrm0q02scamvkVdXyY130_provenance.