Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion type Assertion NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_head.
- NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion description "[We propose that these mutations are the molecular cause of the disease observed in the previously described SCKL2 family and in an additional unrelated family diagnosed with a similar form of congenital microcephaly termed Jawad syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_provenance.
- NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion evidence source_evidence_literature NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_provenance.
- NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion SIO_000772 21998596 NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_provenance.
- NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion wasDerivedFrom befree-20150227 NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_provenance.
- NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_assertion wasGeneratedBy ECO_0000203 NP667548.RALg4wEDlGyG0pf0I3EBk8ZE0J_MB1u2Qusst0hHqzXkw130_provenance.