Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_assertion type Assertion NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_head.
- NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_assertion description "[L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_provenance.
- NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_assertion evidence source_evidence_literature NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_provenance.
- NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_assertion SIO_000772 7920660 NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_provenance.
- NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_assertion wasDerivedFrom befree-2016 NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_provenance.
- NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_assertion wasGeneratedBy ECO_0000203 NP1327002.RAVJjNPV2hR-ydiw5lXtXKRw8CwEjfvoPx6YeEYQtzMLw130_provenance.