Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_assertion> ?p ?o ?g. }
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- NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_assertion type Assertion NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_head.
- NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_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." NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.
- NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_assertion evidence source_evidence_literature NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.
- NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_assertion SIO_000772 25708584 NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.
- NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_assertion wasDerivedFrom befree-2016 NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.
- NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_assertion wasGeneratedBy ECO_0000203 NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.