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- NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_assertion type Assertion NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_head.
- NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_assertion wasGeneratedBy ECO_0000203 NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_provenance.
- NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_assertion wasDerivedFrom befree-20140225 NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_provenance.
- NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_assertion SIO_000772 22927827 NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_provenance.
- NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_assertion evidence source_evidence_literature NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_provenance.
- NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_assertion description "[SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717956.RAfiv3YFTmjdskKbzG2z90botOuOk49qESIPAycg5HyMA130_provenance.