Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_assertion> ?p ?o ?g. }
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- NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_assertion type Assertion NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_head.
- NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_assertion wasGeneratedBy ECO_0000203 NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_provenance.
- NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_assertion wasDerivedFrom befree-20140225 NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_provenance.
- NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_assertion SIO_000772 10822217 NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_provenance.
- NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_assertion evidence source_evidence_literature NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_provenance.
- NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_assertion description "[To characterize clinically and hormonally the syndrome of autosomal recessive familial growth hormone deficiency (FGHD) recently identified in Itabaianinha, Sergipe, Brazil, caused by a novel mutation (mt) that inactivates the growth hormone-releasing hormone receptor (GHRH-R) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP442292.RAzxC2v1FeM83EmD0LbupZNxnp7GA8pIxH824-9-Qdyt4130_provenance.