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- source_evidence_literature type ECO_0000212 NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_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." NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_assertion evidence source_evidence_literature NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_assertion SIO_000772 17941886 NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_assertion wasDerivedFrom befree-20140225 NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_assertion wasGeneratedBy ECO_0000203 NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP379942.RAYlk5BWhvS0CnepBd6hsEo2_FLtF71ReZssetRu026RQ130_provenance.