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- source_evidence_literature type ECO_0000212 NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_assertion description "[Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_assertion evidence source_evidence_literature NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_assertion SIO_000772 17941886 NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_assertion wasDerivedFrom befree-2016 NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_assertion wasGeneratedBy ECO_0000203 NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.
- befree-2016 importedOn "2016-02-19" NP635693.RAcXA-0mjPqa2zzWWQGXjINsTyA0M8aljt8O2sF-gpl6s130_provenance.