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- source_evidence_literature type ECO_0000212 NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1265853.RAymJ43PJE1XjOyoRC4aXhtX3xItC1MvhGG0VMzWEZqrk130_provenance.