Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion> ?p ?o ?g. }
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- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion type Assertion NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_head.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion wasGeneratedBy ECO_0000203 NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion wasDerivedFrom befree-2016 NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion SIO_000772 22344793 NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion evidence source_evidence_literature NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.
- NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_assertion description "[Association of X-linked hydrocephalus and Hirschsprung disease: report of a new patient with a mutation in the L1CAM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961750.RASrnrq0a-nNI1YJJcDsiA56dAZ7UNWlEXwLEn6y4UBXE130_provenance.