Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_assertion> ?p ?o ?g. }
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- NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_assertion type Assertion NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_head.
- NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_assertion description "[How abnormal Ca2+ influx through CaV1.2 underlies phenotypes such as the accompanying syndactyly or craniofacial abnormalities in the majority of affected individuals is not readily explained by established CaV1.2 roles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_provenance.
- NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_assertion evidence source_evidence_literature NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_provenance.
- NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_assertion SIO_000772 23549079 NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_provenance.
- NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_assertion wasDerivedFrom befree-20150227 NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_provenance.
- NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_assertion wasGeneratedBy ECO_0000203 NP277299.RAaMOWdcf9pFw8NLbvhEv_CJp3cAM1ad_T8BQ04_D49Ak130_provenance.