Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_assertion wasGeneratedBy ECO_0000203 NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_assertion wasDerivedFrom befree-20150227 NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_assertion SIO_000772 15148591 NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_assertion evidence source_evidence_literature NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.
- NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_assertion description "[Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768359.RAe2EHYmEwsBq_NVKI0wvSn2eU628Nn6_CL3lDjd5q1_4130_provenance.