Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_assertion> ?p ?o ?g. }
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- NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_assertion type Assertion NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_head.
- NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_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." NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_provenance.
- NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_assertion evidence source_evidence_literature NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_provenance.
- NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_assertion SIO_000772 17941886 NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_provenance.
- NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_assertion wasDerivedFrom befree-2016 NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_provenance.
- NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_assertion wasGeneratedBy ECO_0000203 NP635697.RAiDt8hbfzNCYreZuS2eWutoZ4_mN_ulwxEe58E0fcsNM130_provenance.