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- NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_assertion type Assertion NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_head.
- NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_assertion description "[We identified two novel large deletions in the FBN1 gene in four patients of two unrelated families who met clinical diagnostic criteria for Marfan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_provenance.
- NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_assertion evidence source_evidence_literature NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_provenance.
- NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_assertion SIO_000772 21936929 NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_provenance.
- NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_assertion wasDerivedFrom befree-2016 NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_provenance.
- NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_assertion wasGeneratedBy ECO_0000203 NP925413.RAeb79JOyIsj6_HbRWhcmF9s1QwqDh8Bci7LtXrC_Kf-w130_provenance.