Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_assertion description "[Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_assertion evidence source_evidence_literature NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_assertion SIO_000772 23585173 NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_assertion wasDerivedFrom befree-20150227 NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_assertion wasGeneratedBy ECO_0000203 NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824110.RAISLwbkNK7QVi5bL-uup4_ncybknky2rF5tYW18rmn_k130_provenance.